A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930



Internal ID15548589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:106174190..106206031hg38UCSC Ensembl
Outerchr3:105893037..105924878hg19UCSC Ensembl
Outerchr3:107375727..107407568hg18UCSC Ensembl
Outerchr3:107375727..107407568hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg387664
hg197664
hg187664
hg177664
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10355
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)nsv3930
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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