A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036705



Internal ID19125924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85745502..85793391hg38UCSC Ensembl
Innerchr15:86288733..86336622hg19UCSC Ensembl
Innerchr15:84089737..84137626hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3847890
hg1947890
hg1847890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2650n100
Supporting Variantsnssv3555081
Samples
Known GenesAKAP13, KLHL25, MIR1276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036705
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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