A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969705



Internal ID18868406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:47449177..47451950hg38UCSC Ensembl
Outerchr3:47490667..47493440hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382774
hg192774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123645
Supporting Variants
SamplesKWS1
Known GenesSCAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969705
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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