A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765



Internal ID15549507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:24629232..24659295hg38UCSC Ensembl
Outerchr5:24629341..24659404hg19UCSC Ensembl
Outerchr5:24665098..24695161hg18UCSC Ensembl
Outerchr5:24665098..24695161hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg389424
hg199424
hg189424
hg179424
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10446
SamplesNA18956
Known GenesCDH10
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)nsv4765
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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