A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5155



Internal ID15549936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:178648099..178705798hg38UCSC Ensembl
Outerchr5:178075100..178132799hg19UCSC Ensembl
Outerchr5:178007706..178065405hg18UCSC Ensembl
Outerchr5:178007706..178065405hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857700
hg1957700
hg1857700
hg1757700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8205, nssv3408, nssv2560
SamplesNA12156, NA12878, NA18555
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)nsv5155
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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