A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149331



Internal ID15530887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83997830..84008053hg38UCSC Ensembl
Innerchr16:84031435..84041658hg19UCSC Ensembl
Innerchr16:82588936..82599159hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810224
hg1910224
hg1810224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573417
Supporting Variants
SamplesHGDP01009
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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