A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955935



Internal ID19206685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:109199333..109199849hg38UCSC Ensembl
Outerchr2:109815789..109816305hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136394
Supporting Variants
SamplesKWS1
Known GenesSH3RF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955935
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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