A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv433



Internal ID15544941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183862512..183875576hg38UCSC Ensembl
Outerchr4:184783665..184796729hg19UCSC Ensembl
Outerchr4:185020659..185033723hg18UCSC Ensembl
Outerchr4:185158814..185171878hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385874
hg195874
hg185874
hg175874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4636
Supporting Variants
SamplesNA19240
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)nssv433
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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