A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991897



Internal ID18897216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:83300555..83300840hg38UCSC Ensembl
Outerchr4:84221708..84221993hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139276
Supporting Variants
SamplesKWS2
Known GenesHPSE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991897
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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