A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028544



Internal ID19117762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84491086..84614971hg38UCSC Ensembl
Innerchr5:83786904..83910789hg19UCSC Ensembl
Innerchr5:83822660..83946545hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38123886
hg19123886
hg18123886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5710n100
Supporting Variantsnssv3639155
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)nsv1028544
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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