A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721581



Internal ID18673176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30790060hg38UCSC Ensembl
Innerchr15:30900866..31082263hg19UCSC Ensembl
Innerchr15:28688158..28869555hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38181398
hg19181398
hg18181398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048016
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)nssv3721581
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer