A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021972



Internal ID18764506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17011649..17091769hg38UCSC Ensembl
Innerchr5:17011758..17091878hg19UCSC Ensembl
Innerchr5:17064758..17144878hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3880121
hg1980121
hg1880121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638305
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021972
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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