A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862592



Internal ID15809862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88534417..88547875hg38UCSC Ensembl
Innerchr16:88600825..88614283hg19UCSC Ensembl
Innerchr16:87128326..87141784hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3813459
hg1913459
hg1813459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573609
Supporting Variants
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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