A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520842



Internal ID15101449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28130831..28133779hg38UCSC Ensembl
Innerchr10:28419760..28422708hg19UCSC Ensembl
Innerchr10:28459766..28462714hg18UCSC Ensembl
Innerchr10:28459766..28462714hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382949
hg192949
hg182949
hg172949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676314, nssv688923, nssv684159, nssv685025
Samples
Known GenesMPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520842
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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