A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967826



Internal ID18888183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89618792..89619992hg38UCSC Ensembl
Outerchr16:89685200..89686400hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131122
Supporting Variants
SamplesKWS2
Known GenesDPEP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967826
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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