A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546467



Internal ID18498062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30795118hg38UCSC Ensembl
Innerchr15:30386399..31087321hg19UCSC Ensembl
Innerchr15:28173691..28874613hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38700923
hg19700923
hg18700923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049639
Supporting Variants
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3546467
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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