A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3711



Internal ID15201662
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 StatusM
Merged Variants
Supporting Variantsnssv1658
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)nsv3711
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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