A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035049



Internal ID19124268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:62732168..63580003hg38UCSC Ensembl
Innerchr5:62027995..62875830hg19UCSC Ensembl
Innerchr5:62063751..62911586hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38847836
hg19847836
hg18847836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5691n100
Supporting Variantsnssv3640785
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)nsv1035049
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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