A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966803



Internal ID19228546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165081465..165083903hg38UCSC Ensembl
Outerchr4:166002617..166005055hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130492
Supporting Variants
SamplesKWS2
Known GenesTMEM192
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966803
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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