A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042724



Internal ID19131943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68123405..68165710hg38UCSC Ensembl
Innerchr15:68415743..68458048hg19UCSC Ensembl
Innerchr15:66202797..66245102hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3842306
hg1942306
hg1842306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553657
Samples
Known GenesPIAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042724
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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