A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957429



Internal ID18871226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:189966083..189966152hg38UCSC Ensembl
Outerchr3:189683872..189683941hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128012
Supporting Variants
SamplesKWS1
Known GenesLEPREL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957429
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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