A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156220



Internal ID15508975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6567841..7017391hg38UCSC Ensembl
Innerchr9:6567841..7017391hg19UCSC Ensembl
Innerchr9:6557841..7007391hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38449551
hg19449551
hg18449551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613208
Supporting Variants
Samples1782681216_A
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156220
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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