A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857279



Internal ID16151235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49855020..49858537hg38UCSC Ensembl
Innerchr16:49888931..49892448hg19UCSC Ensembl
Innerchr16:48446432..48449949hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383518
hg193518
hg183518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572582
Supporting Variants
Samples
Known GenesZNF423
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv857279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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