A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9634



Internal ID15540169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186207632..186219707hg38UCSC Ensembl
Outerchr3:185925421..185937496hg19UCSC Ensembl
Outerchr3:187408115..187420190hg18UCSC Ensembl
Outerchr3:187408123..187420198hg17UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3824624
hg1924624
hg1824624
hg1724624
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4150
Supporting Variants
SamplesNA18507
Known GenesDGKG
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)nssv9634
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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