A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017193



Internal ID19106410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12345905..12503256hg38UCSC Ensembl
Innerchr5:12346017..12503368hg19UCSC Ensembl
Innerchr5:12399017..12556368hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38157352
hg19157352
hg18157352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638206
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)nsv1017193
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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