A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547634



Internal ID18499229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30628409..30785538hg38UCSC Ensembl
Innerchr15:30920612..31077741hg19UCSC Ensembl
Innerchr15:28707904..28865033hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38157130
hg19157130
hg18157130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041226
Supporting Variants
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547634
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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