A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156209



Internal ID15875241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4743477..4758022hg38UCSC Ensembl
Innerchr9:4743477..4758022hg19UCSC Ensembl
Innerchr9:4733477..4748022hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3814546
hg1914546
hg1814546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613174
Supporting Variants
SamplesHGDP00655
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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