A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028629



Internal ID19117847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46195769..46389159hg38UCSC Ensembl
Innerchr5:46195871..46389261hg19UCSC Ensembl
Innerchr5:46231628..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38193391
hg19193391
hg18193391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5649n100
Supporting Variantsnssv3637986
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)nsv1028629
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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