A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016440



Internal ID19105659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8704363..8752606hg38UCSC Ensembl
Innerchr5:8704475..8752718hg19UCSC Ensembl
Innerchr5:8757475..8805718hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3848244
hg1948244
hg1848244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3746432
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)nsv1016440
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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