A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049643



Internal ID19138862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36536513..36550849hg38UCSC Ensembl
Innerchr15:36828714..36843050hg19UCSC Ensembl
Innerchr15:34616006..34630342hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3814337
hg1914337
hg1814337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552235
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)nsv1049643
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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