A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016368



Internal ID19105587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53311906..53345156hg38UCSC Ensembl
Innerchr5:52607736..52640986hg19UCSC Ensembl
Innerchr5:52643493..52676743hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3833251
hg1933251
hg1833251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5667n100
Supporting Variantsnssv3642130
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)nsv1016368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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