A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025213



Internal ID16319169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10563087..10564360hg38UCSC Ensembl
Innerchr5:10563199..10564472hg19UCSC Ensembl
Innerchr5:10616199..10617472hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381274
hg191274
hg181274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597121
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)nssv1025213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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