A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046337



Internal ID18788868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85268380..85430662hg38UCSC Ensembl
Innerchr15:85811611..85973893hg19UCSC Ensembl
Innerchr15:83612615..83774897hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38162283
hg19162283
hg18162283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2647n100
Supporting Variantsnssv3555065
Samples
Known GenesAKAP13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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