A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513503



Internal ID18465098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133282503..133353665hg38UCSC Ensembl
Innerchr10:135096007..135167169hg19UCSC Ensembl
Innerchr10:134945997..135017159hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3871163
hg1971163
hg1871163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040726
Supporting Variants
Samples
Known GenesCALY, PRAP1, TUBGCP2, ZNF511
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513503
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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