A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026188



Internal ID19115405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145147630..145187643hg38UCSC Ensembl
Innerchr5:144527193..144567206hg19UCSC Ensembl
Innerchr5:144507386..144547399hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3840014
hg1940014
hg1840014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5816n100
Supporting Variantsnssv3648156
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)nsv1026188
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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