A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4815



Internal ID15202876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:42973448..43006068hg38UCSC Ensembl
Outerchr5:42973550..43006170hg19UCSC Ensembl
Outerchr5:43009307..43041927hg18UCSC Ensembl
Outerchr5:43009307..43041927hg17UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg387116
hg197116
hg187116
hg177116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3347
SamplesNA12878
Known GenesFLJ32255
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)nsv4815
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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