A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547621



Internal ID18499216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30777478hg38UCSC Ensembl
Innerchr15:30900866..31069681hg19UCSC Ensembl
Innerchr15:28688158..28856973hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38168816
hg19168816
hg18168816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043971
Supporting Variants
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547621
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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