A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610714



Internal ID6997631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126726836..126732735hg38UCSC Ensembl
Innerchr6:126726847..126732724hg38UCSC Ensembl
Outerchr6:126726825..126732746hg38UCSC Ensembl
chr6:127047981..127053880hg19UCSC Ensembl
Innerchr6:127047992..127053869hg19UCSC Ensembl
Outerchr6:127047970..127053891hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12540710, essv12540711
SamplesHG00332, NA18516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610714
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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