A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999063



Internal ID18844300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89648687..89648840hg38UCSC Ensembl
Outerchr16:89715095..89715248hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151881
Supporting Variants
SamplesKWB1
Known GenesCHMP1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999063
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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