A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609075



Internal ID6995997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55620708..55627976hg38UCSC Ensembl
Innerchr6:55620773..55627912hg38UCSC Ensembl
Outerchr6:55620644..55628041hg38UCSC Ensembl
chr6:55485506..55492774hg19UCSC Ensembl
Innerchr6:55485571..55492710hg19UCSC Ensembl
Outerchr6:55485442..55492839hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg387269
hg197269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12363364
SamplesHG00313
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609075
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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