A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609261



Internal ID6996183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63485576..63488607hg38UCSC Ensembl
Innerchr6:63485591..63488593hg38UCSC Ensembl
Outerchr6:63485562..63488622hg38UCSC Ensembl
chr6:64195481..64198512hg19UCSC Ensembl
Innerchr6:64195496..64198498hg19UCSC Ensembl
Outerchr6:64195467..64198527hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg383032
hg193032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389797
SamplesHG03963
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609261
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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