A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176519



Internal ID15873943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133633021..133640119hg38UCSC Ensembl
Innerchr9:136498143..136505241hg19UCSC Ensembl
Innerchr9:135487964..135495062hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387099
hg197099
hg187099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615638
Supporting Variants
SamplesHGDP00445
Known GenesDBH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176519
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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