A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9876



Internal ID15539951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184431472..184443963hg38UCSC Ensembl
Outerchr3:184149260..184161751hg19UCSC Ensembl
Outerchr3:185631954..185644445hg18UCSC Ensembl
Outerchr3:185631962..185644453hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg387345
hg197345
hg187345
hg177345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4147
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9876
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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