A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040998



Internal ID19130217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85272369..85563566hg38UCSC Ensembl
Innerchr15:85815600..86106797hg19UCSC Ensembl
Innerchr15:83616604..83907801hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38291198
hg19291198
hg18291198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2648n100
Supporting Variantsnssv3555074
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)nsv1040998
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer