A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1668



Internal ID15198711
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 StatusS
Merged Variantsnsv3761
Supporting Variants
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)nssv1668
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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