A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051867



Internal ID19141086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85745502..85801191hg38UCSC Ensembl
Innerchr15:86288733..86344422hg19UCSC Ensembl
Innerchr15:84089737..84145426hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3855690
hg1955690
hg1855690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2650n100
Supporting Variantsnssv3555082
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)nsv1051867
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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