A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839444



Internal ID15786714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30089917..30626045hg38UCSC Ensembl
Innerchr15:30382120..30918248hg19UCSC Ensembl
Innerchr15:28169412..28705540hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38536129
hg19536129
hg18536129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568718
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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