A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv341



Internal ID15198452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151879925..151910130hg38UCSC Ensembl
Outerchr3:151597713..151627918hg19UCSC Ensembl
Outerchr3:153080403..153110608hg18UCSC Ensembl
Outerchr3:153080411..153110616hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3810795
hg1910795
hg1810795
hg1710795
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4067
Supporting Variants
SamplesNA19240
Known GenesSUCNR1
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)nssv341
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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