A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4780



Internal ID15543167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:120201022..120223899hg38UCSC Ensembl
Outerchr4:121122177..121145054hg19UCSC Ensembl
Outerchr4:121341627..121364504hg18UCSC Ensembl
Outerchr4:121479782..121502659hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg387170
hg197170
hg187170
hg177170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4489
Supporting Variants
SamplesNA19129
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)nssv4780
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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