A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035336



Internal ID19124555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85745502..85775555hg38UCSC Ensembl
Innerchr15:86288733..86318786hg19UCSC Ensembl
Innerchr15:84089737..84119790hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3830054
hg1930054
hg1830054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2649n100
Supporting Variantsnssv3555080
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)nsv1035336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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