A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029870



Internal ID19119089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:125942641..125972835hg38UCSC Ensembl
Innerchr5:125278334..125308528hg19UCSC Ensembl
Innerchr5:125306233..125336427hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3830195
hg1930195
hg1830195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648096
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)nsv1029870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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