A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637175



Internal ID7023969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88710831..88712988hg38UCSC Ensembl
Innerchr15:88710832..88712988hg38UCSC Ensembl
Outerchr15:88710831..88712989hg38UCSC Ensembl
chr15:89254062..89256219hg19UCSC Ensembl
Innerchr15:89254063..89256219hg19UCSC Ensembl
Outerchr15:89254062..89256220hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382158
hg192158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15316926, essv15316937, essv15316929, essv15316925, essv15316940, essv15316936, essv15316920, essv15316931, essv15316933, essv15316934, essv15316921, essv15316922, essv15316938, essv15316944, essv15316941, essv15316942, essv15316932, essv15316918, essv15316919, essv15316923, essv15316948, essv15316945, essv15316928, essv15316924, essv15316939, essv15316927, essv15316935, essv15316917, essv15316943, essv15316916, essv15316946, essv15316947, essv15316930
SamplesNA20874, NA20877, HG03731, HG04222, NA21092, NA21115, HG03680, HG03782, HG03722, HG03808, HG03490, HG02491, HG04206, HG02786, HG03986, HG03968, HG03888, HG03744, HG03714, NA21118, NA20867, HG03730, HG03713, HG04159, HG03694, HG04200, HG04216, HG03920, HG03716, HG04098, HG02774, HG03931, HG03989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637175
Frequency
Sample Size2504
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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