A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025219



Internal ID16319175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10636310..10639396hg38UCSC Ensembl
Innerchr5:10636422..10639508hg19UCSC Ensembl
Innerchr5:10689422..10692508hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg383087
hg193087
hg183087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597126
Supporting Variants
Samples
Known GenesANKRD33B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1025219
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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