A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546688



Internal ID18498283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30274687..30633390hg38UCSC Ensembl
Innerchr15:30566890..30925593hg19UCSC Ensembl
Innerchr15:28354182..28712885hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38358704
hg19358704
hg18358704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054935
Supporting Variants
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, LOC101059918, 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)nssv3546688
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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