A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608835



Internal ID6995759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44680722..44683370hg38UCSC Ensembl
Innerchr6:44680749..44683343hg38UCSC Ensembl
Outerchr6:44680695..44683397hg38UCSC Ensembl
chr6:44648459..44651107hg19UCSC Ensembl
Innerchr6:44648486..44651080hg19UCSC Ensembl
Outerchr6:44648432..44651134hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12333296
SamplesHG03895
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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