A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025795



Internal ID19115012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27143176..27199483hg38UCSC Ensembl
Innerchr5:27143283..27199590hg19UCSC Ensembl
Innerchr5:27179040..27235347hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3856308
hg1956308
hg1856308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5609n100
Supporting Variantsnssv3635965
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)nsv1025795
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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