A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844319



Internal ID16138275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67010301..67055348hg38UCSC Ensembl
Innerchr15:67302639..67347686hg19UCSC Ensembl
Innerchr15:65089693..65134740hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3845048
hg1945048
hg1845048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569795
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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