A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029468



Internal ID19118687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101008550..101177623hg38UCSC Ensembl
Innerchr5:100344254..100513327hg19UCSC Ensembl
Innerchr5:100372153..100541226hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38169074
hg19169074
hg18169074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645801
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)nsv1029468
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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