A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017337



Internal ID19106554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103700839..103752591hg38UCSC Ensembl
Innerchr5:103036540..103088292hg19UCSC Ensembl
Innerchr5:103064439..103116191hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3851753
hg1951753
hg1851753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5752n100
Supporting Variantsnssv3645915
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)nsv1017337
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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