A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605837



Internal ID6646081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706469..95713312hg38UCSC Ensembl
chr5:95042173..95049016hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386844
hg196844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112e214
Supporting Variantsessv11983063, essv11983061, essv11983060, essv11983058, essv11983057, essv11983059, essv11983062
SamplesHG01815, NA19717, HG04054, HG02408, HG02019, HG01804, HG02462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605837
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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