A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852779



Internal ID15800049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14693063..14742768hg38UCSC Ensembl
Innerchr16:14786920..14836625hg19UCSC Ensembl
Innerchr16:14694421..14744126hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3849706
hg1949706
hg1849706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571509
Supporting Variants
Samples
Known GenesNPIPA2, NPIPA3, PLA2G10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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