A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120819



Internal ID19281497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1601223..1601954hg38UCSC Ensembl
Outerchr4:1602950..1603681hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2707n106
Supporting Variantsnssv3963261
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120819
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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