A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4471



Internal ID15202498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112573142..112605752hg38UCSC Ensembl
Outerchr4:113494298..113526908hg19UCSC Ensembl
Outerchr4:113713747..113746357hg18UCSC Ensembl
Outerchr4:113851902..113884512hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3832611
hg1932611
hg1832611
hg1732611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2477
SamplesNA18555
Known GenesC4orf21
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)nsv4471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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