A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4705



Internal ID15202755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:7895073..7927282hg38UCSC Ensembl
Outerchr5:7895186..7927395hg19UCSC Ensembl
Outerchr5:7948186..7980395hg18UCSC Ensembl
Outerchr5:7948186..7980395hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg387228
hg197228
hg187228
hg177228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7145
SamplesNA12156
Known GenesMTRR
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)nsv4705
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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