A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4773



Internal ID15549516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:28774129..28808318hg38UCSC Ensembl
Outerchr5:28774236..28808425hg19UCSC Ensembl
Outerchr5:28809993..28844182hg18UCSC Ensembl
Outerchr5:28809993..28844182hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg385235
hg195235
hg185235
hg175235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8086
SamplesNA12156
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)nsv4773
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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