A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3237



Internal ID15537965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:13986900..14021859hg38UCSC Ensembl
Outerchr4:13988524..14023483hg19UCSC Ensembl
Outerchr4:13597622..13632581hg18UCSC Ensembl
Outerchr4:13664793..13699752hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg384736
hg194736
hg184736
hg174736
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4241
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)nssv3237
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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