A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974746



Internal ID19227151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:41783343..41783406hg38UCSC Ensembl
Outerchr4:41785360..41785423hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136841
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974746
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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