A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176503



Internal ID15533756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129687477..129735271hg38UCSC Ensembl
Innerchr9:132449756..132497550hg19UCSC Ensembl
Innerchr9:131489577..131537371hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3847795
hg1947795
hg1847795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615497
Supporting Variants
SamplesNINDS_210
Known GenesPRRX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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