A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176506



Internal ID15854676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130158297..130200850hg38UCSC Ensembl
Innerchr9:132920576..132963129hg19UCSC Ensembl
Innerchr9:131960397..132002950hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3842554
hg1942554
hg1842554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615501
Supporting Variants
Samples1780862275_A
Known GenesNCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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