A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025214



Internal ID16319170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10563087..10565264hg38UCSC Ensembl
Innerchr5:10563199..10565376hg19UCSC Ensembl
Innerchr5:10616199..10618376hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382178
hg192178
hg182178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597122
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)nssv1025214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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