A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969887



Internal ID19229958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:66910809..66910917hg38UCSC Ensembl
Outerchr16:66944712..66944820hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113815
Supporting Variants
SamplesKWS2
Known GenesCDH16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969887
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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