A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442



Internal ID15202466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:102498046..102529664hg38UCSC Ensembl
Outerchr4:103419203..103450821hg19UCSC Ensembl
Outerchr4:103638235..103669851hg18UCSC Ensembl
Outerchr4:103776390..103808006hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg387886
hg197886
hg187886
hg177886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10417
SamplesNA18956
Known GenesNFKB1
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)nsv4442
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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