A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1658



Internal ID15198722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13906341..13938097hg38UCSC Ensembl
Outerchr3:13947838..13979597hg19UCSC Ensembl
Outerchr3:13922839..13954598hg18UCSC Ensembl
Outerchr3:13922839..13954598hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386238
hg196238
hg186238
hg176238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3711
Supporting Variants
SamplesNA19240
Known GenesFGD5P1, TPRXL
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)nssv1658
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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