A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021895



Internal ID19111113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17630..55354hg38UCSC Ensembl
Innerchr5:17630..55469hg19UCSC Ensembl
Innerchr5:70630..108469hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3837725
hg1937840
hg1837840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5511n100
Supporting Variantsnssv3636545, nssv3636546
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)nsv1021895
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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