A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149324



Internal ID15533478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83625405..83631037hg38UCSC Ensembl
Innerchr16:83659010..83664642hg19UCSC Ensembl
Innerchr16:82216511..82222143hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385633
hg195633
hg185633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573400
Supporting Variants
SamplesNINDS_166
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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