A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957084



Internal ID19203769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:4793706..4793757hg38UCSC Ensembl
Outerchr4:4795433..4795484hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109575
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957084
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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