A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126033



Internal ID15979219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:924525..953280hg38UCSC Ensembl
Innerchr9:924525..953280hg19UCSC Ensembl
Innerchr9:914525..943280hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3828756
hg1928756
hg1828756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613048
Supporting Variants
Samples
Known GenesDMRT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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