A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3202



Internal ID15537930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:138825365..138860669hg38UCSC Ensembl
Outerchr3:138544207..138579511hg19UCSC Ensembl
Outerchr3:140026897..140062201hg18UCSC Ensembl
Outerchr3:140026905..140062209hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384432
hg194432
hg184432
hg174432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4031
Supporting Variants
SamplesNA12878
Known Genes
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)nssv3202
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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