A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991857



Internal ID19226687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:43101704..43101762hg38UCSC Ensembl
Outerchr4:43103721..43103779hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139237
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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