A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858146



Internal ID16152102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58035317..58046468hg38UCSC Ensembl
Innerchr16:58069221..58080372hg19UCSC Ensembl
Innerchr16:56626722..56637873hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3811152
hg1911152
hg1811152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572761
Supporting Variants
Samples
Known GenesMMP15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv858146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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