A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547602



Internal ID18499197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30487376..30688830hg38UCSC Ensembl
Innerchr15:30779579..30981033hg19UCSC Ensembl
Innerchr15:28566871..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38201455
hg19201455
hg18201455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038251
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)nssv3547602
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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