A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663964



Internal ID15400616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68309040..68309476hg38UCSC Ensembl
Innerchr10:70068797..70069233hg19UCSC Ensembl
Innerchr10:69738803..69739239hg18UCSC Ensembl
Innerchr10:69738803..69739239hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38437
hg19437
hg18437
hg17437
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517615
Supporting Variants
Samples
Known GenesPBLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663964
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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