A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3842



Internal ID15548492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:59785151..59814731hg38UCSC Ensembl
Outerchr3:59770877..59800457hg19UCSC Ensembl
Outerchr3:59745917..59775497hg18UCSC Ensembl
Outerchr3:59745917..59775497hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3810167
hg1910167
hg1810167
hg1710167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3168
SamplesNA12878
Known GenesFHIT
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)nsv3842
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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