A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515591



Internal ID18467186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121986932..122086108hg38UCSC Ensembl
Innerchr10:123746447..123845623hg19UCSC Ensembl
Innerchr10:123736437..123835613hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3899177
hg1999177
hg1899177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045815
Supporting Variants
Samples
Known GenesTACC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515591
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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