A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613270



Internal ID16400679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7856992..7889991hg38UCSC Ensembl
Innerchr9:7856992..7889991hg19UCSC Ensembl
Innerchr9:7846992..7879991hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3833000
hg1933000
hg1833000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156229
SamplesHGDP01032
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613270
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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