A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971686



Internal ID19221905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:119944342..119945446hg38UCSC Ensembl
Outerchr4:120865497..120866601hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134203
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971686
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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