A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986331



Internal ID19219370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38753591..38753650hg38UCSC Ensembl
Outerchr4:38755212..38755271hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131786
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986331
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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