A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032835



Internal ID18775369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19572..132055hg38UCSC Ensembl
Innerchr5:19572..132170hg19UCSC Ensembl
Innerchr5:72572..185170hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38112484
hg19112599
hg18112599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5517n100
Supporting Variantsnssv3633201
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)nsv1032835
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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