A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546765



Internal ID18845046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313356..30796262hg38UCSC Ensembl
Innerchr15:30605559..31088465hg19UCSC Ensembl
Innerchr15:28392851..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38482907
hg19482907
hg18482907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054601
Supporting Variants
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3546765
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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