A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053813



Internal ID18796344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30483779..30687726hg38UCSC Ensembl
Innerchr15:30775982..30979929hg19UCSC Ensembl
Innerchr15:28563274..28767221hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38203948
hg19203948
hg18203948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2525n100
Supporting Variantsnssv3721575
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)nsv1053813
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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