A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv721166



Internal ID15668436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108873603..109035828hg38UCSC Ensembl
Innerchr1:109416225..109578450hg19UCSC Ensembl
Innerchr1:109217748..109379973hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38162226
hg19162226
hg18162226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547425
Supporting Variants
Samples
Known GenesCLCC1, GPSM2, WDR47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv721166
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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