A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047174



Internal ID18789705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30376250..30628409hg38UCSC Ensembl
Innerchr15:30668453..30920612hg19UCSC Ensembl
Innerchr15:28455745..28707904hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38252160
hg19252160
hg18252160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2520n100
Supporting Variantsnssv3547571
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)nsv1047174
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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