A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027559



Internal ID19116778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5717261hg38UCSC Ensembl
Innerchr5:5682532..5717374hg19UCSC Ensembl
Innerchr5:5735532..5770374hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3834843
hg1934843
hg1834843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5555n100
Supporting Variantsnssv3638589, nssv3638590, nssv3638587, nssv3638588
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)nsv1027559
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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