A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613762



Internal ID7000657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76395994..76401667hg38UCSC Ensembl
Innerchr7:76396144..76401517hg38UCSC Ensembl
Outerchr7:76395844..76401817hg38UCSC Ensembl
chr7:76025311..76030984hg19UCSC Ensembl
Innerchr7:76025461..76030834hg19UCSC Ensembl
Outerchr7:76025161..76031134hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385674
hg195674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848882
SamplesHG03697
Known GenesSRCRB4D, ZP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613762
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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