A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033562



Internal ID18776095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36927550..36994709hg38UCSC Ensembl
Innerchr5:36927652..36994811hg19UCSC Ensembl
Innerchr5:36963409..37030568hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3867160
hg1967160
hg1867160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3637074
Samples
Known GenesNIPBL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033562
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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