A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10373



Internal ID15542425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:163698847..163722463hg38UCSC Ensembl
Outerchr3:163416635..163440251hg19UCSC Ensembl
Outerchr3:164899329..164922945hg18UCSC Ensembl
Outerchr3:164899337..164922953hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg387706
hg197706
hg187706
hg177706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4097
Supporting Variants
SamplesNA18956
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)nssv10373
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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