A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026356



Internal ID19115574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5790815..5808943hg38UCSC Ensembl
Innerchr5:5790928..5809056hg19UCSC Ensembl
Innerchr5:5843928..5862056hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3818129
hg1918129
hg1818129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638596
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)nsv1026356
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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