A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613763



Internal ID7000658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76411814..76418445hg38UCSC Ensembl
Innerchr7:76411814..76418445hg38UCSC Ensembl
Outerchr7:76411684..76418626hg38UCSC Ensembl
chr7:76041131..76047762hg19UCSC Ensembl
Innerchr7:76041131..76047762hg19UCSC Ensembl
Outerchr7:76041001..76047943hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386632
hg196632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848884, essv12848883
SamplesHG00251, NA19917
Known GenesZP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613763
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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