A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991727



Internal ID19236737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:35667840..35667939hg38UCSC Ensembl
Outerchr3:35709332..35709431hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139105
Supporting Variants
SamplesKWS2
Known GenesARPP21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991727
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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