A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156759



Internal ID15532251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28649449..28942610hg38UCSC Ensembl
Innerchr9:28649447..28942608hg19UCSC Ensembl
Innerchr9:28639447..28932608hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38293162
hg19293162
hg18293162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614005
Supporting Variants
SamplesHGDP01281
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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