A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506936



Internal ID18805217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52774542..52789557hg38UCSC Ensembl
Innerchr10:54534302..54549317hg19UCSC Ensembl
Innerchr10:54204308..54219323hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3815016
hg1915016
hg1815016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038975
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506936
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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