A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957034



Internal ID19214417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:123473098..123473162hg38UCSC Ensembl
Outerchr3:123191945..123192009hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109543
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957034
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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