A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704689



Internal ID15441341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77275140..77288849hg38UCSC Ensembl
Innerchr13:77849275..77862984hg19UCSC Ensembl
Innerchr13:76747276..76760985hg18UCSC Ensembl
Innerchr13:76747276..76760985hg17UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3813710
hg1913710
hg1813710
hg1713710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528143
Supporting Variants
Samples
Known GenesMYCBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704689
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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