A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553659



Internal ID18505254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68312766..68350422hg38UCSC Ensembl
Innerchr15:68605104..68642760hg19UCSC Ensembl
Innerchr15:66392158..66429814hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3837657
hg1937657
hg1837657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039597
Supporting Variants
Samples
Known GenesITGA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3553659
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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