A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610027



Internal ID6996946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94677185..94878840hg38UCSC Ensembl
Innerchr6:94677685..94878340hg38UCSC Ensembl
Outerchr6:94676185..94879840hg38UCSC Ensembl
chr6:95386903..95588558hg19UCSC Ensembl
Innerchr6:95387403..95588058hg19UCSC Ensembl
Outerchr6:95385903..95589558hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38201656
hg19201656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12469605, essv12469608, essv12469604, essv12469603, essv12469607, essv12469606, essv12469609
SamplesNA19393, NA19338, HG02139, HG00171, HG02284, HG00180, NA20908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610027
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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