A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668530



Internal ID15405182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79041189..79043121hg38UCSC Ensembl
Innerchr10:80800946..80802878hg19UCSC Ensembl
Innerchr10:80470952..80472884hg18UCSC Ensembl
Innerchr10:80470952..80472884hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381933
hg191933
hg181933
hg171933
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516458
Supporting Variants
Samples
Known GenesZMIZ1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668530
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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