A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1665



Internal ID15198714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32966390..32999973hg38UCSC Ensembl
Outerchr3:33007882..33041465hg19UCSC Ensembl
Outerchr3:32982886..33016469hg18UCSC Ensembl
Outerchr3:32982886..33016469hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg387413
hg197413
hg187413
hg177413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3753
Supporting Variants
SamplesNA19240
Known GenesGLB1
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)nssv1665
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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