A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842980



Internal ID16136936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51499362..51598085hg38UCSC Ensembl
Innerchr15:51791559..51890282hg19UCSC Ensembl
Innerchr15:49578851..49677574hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3898724
hg1998724
hg1898724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569405
Supporting Variants
Samples
Known GenesDMXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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