A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984260



Internal ID19225070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:184962287..184962371hg38UCSC Ensembl
Outerchr4:185883441..185883525hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126052
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984260
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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