A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043693



Internal ID18786224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59652272..59679301hg38UCSC Ensembl
Innerchr15:59944471..59971500hg19UCSC Ensembl
Innerchr15:57731763..57758792hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3827030
hg1927030
hg1827030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553615
Samples
Known GenesBNIP2, GTF2A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043693
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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