A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981038



Internal ID19220256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:81444495..81447295hg38UCSC Ensembl
Outerchr16:81478100..81480900hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118357
Supporting Variants
SamplesKWS1
Known GenesCMIP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981038
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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