A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4633



Internal ID15549362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183407005..183442012hg38UCSC Ensembl
Outerchr4:184328158..184363165hg19UCSC Ensembl
Outerchr4:184565152..184600159hg18UCSC Ensembl
Outerchr4:184703307..184738314hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385976
hg195976
hg185976
hg175976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv432
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)nsv4633
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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