A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134061



Internal ID15987247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38620378..38621733hg38UCSC Ensembl
Innerchr9:38620375..38621730hg19UCSC Ensembl
Innerchr9:38610375..38611730hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614272
Supporting Variants
Samples
Known GenesFAM201A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134061
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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