A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686096



Internal ID15076062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275803..28282931hg38UCSC Ensembl
Innerchr10:28564732..28571860hg19UCSC Ensembl
Innerchr10:28604738..28611866hg18UCSC Ensembl
Innerchr10:28604738..28611866hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg387129
hg197129
hg187129
hg177129
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515548
Supporting Variants
Samples
Known GenesMPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686096
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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