A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176505



Internal ID15877649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130156951..130206355hg38UCSC Ensembl
Innerchr9:132919230..132968634hg19UCSC Ensembl
Innerchr9:131959051..132008455hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3849405
hg1949405
hg1849405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615500
Supporting Variants
SamplesHGDP01023
Known GenesNCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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