A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942



Internal ID15548602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:110978854..111013430hg38UCSC Ensembl
Outerchr3:110697701..110732277hg19UCSC Ensembl
Outerchr3:112180391..112214967hg18UCSC Ensembl
Outerchr3:112180391..112214967hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg386411
hg196411
hg186411
hg176411
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv316
SamplesNA19240
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)nsv3942
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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