A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3761



Internal ID15201717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36406704..36439909hg38UCSC Ensembl
Outerchr3:36448196..36481401hg19UCSC Ensembl
Outerchr3:36423200..36456405hg18UCSC Ensembl
Outerchr3:36423200..36456405hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg387777
hg197777
hg187777
hg177777
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1668
SamplesNA19240
Known GenesSTAC
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)nsv3761
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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