A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12848884



Internal ID6318651
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613763
Supporting Variants
SamplesNA19917
Known GenesZP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12848884
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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