A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721579



Internal ID18673174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30487376..30796262hg38UCSC Ensembl
Innerchr15:30779579..31088465hg19UCSC Ensembl
Innerchr15:28566871..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38308887
hg19308887
hg18308887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054817
Supporting Variants
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, 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)nssv3721579
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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