A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1655



Internal ID15198725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10834085..10867396hg38UCSC Ensembl
Outerchr3:10875770..10909081hg19UCSC Ensembl
Outerchr3:10850770..10884081hg18UCSC Ensembl
Outerchr3:10850770..10884081hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg387687
hg197687
hg187687
hg177687
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3696
Supporting Variants
SamplesNA19240
Known GenesSLC6A11
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)nssv1655
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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