A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049177



Internal ID18791708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30304080..30638297hg38UCSC Ensembl
Innerchr15:30596283..30930500hg19UCSC Ensembl
Innerchr15:28383575..28717792hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38334218
hg19334218
hg18334218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2514n100
Supporting Variantsnssv3546745
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)nsv1049177
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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