A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607939



Internal ID6994870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3955589..3957569hg38UCSC Ensembl
Innerchr6:3955592..3957566hg38UCSC Ensembl
Outerchr6:3955586..3957572hg38UCSC Ensembl
chr6:3955823..3957803hg19UCSC Ensembl
Innerchr6:3955826..3957800hg19UCSC Ensembl
Outerchr6:3955820..3957806hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179404, essv12179403, essv12179405
SamplesNA19395, NA19390, HG01342
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607939
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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