A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608267



Internal ID6995197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19223343..19249447hg38UCSC Ensembl
Innerchr6:19223493..19249297hg38UCSC Ensembl
Outerchr6:19223193..19249597hg38UCSC Ensembl
chr6:19223574..19249678hg19UCSC Ensembl
Innerchr6:19223724..19249528hg19UCSC Ensembl
Outerchr6:19223424..19249828hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3826105
hg1926105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12213545, essv12213543, essv12213539, essv12213544, essv12213540, essv12213542, essv12213541
SamplesNA19819, HG02325, HG03786, HG03124, HG03833, NA18909, HG02970
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608267
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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