A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969902



Internal ID18891384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:84870454..84870523hg38UCSC Ensembl
Outerchr16:84904060..84904129hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113825
Supporting Variants
SamplesKWS2
Known GenesCRISPLD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969902
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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