A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659



Internal ID15550490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:22584816..22618644hg38UCSC Ensembl
Outerchr7:22624435..22658263hg19UCSC Ensembl
Outerchr7:22590960..22624788hg18UCSC Ensembl
Outerchr7:22397675..22431503hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385428
hg195428
hg185428
hg175428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4972
SamplesNA19129
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)nsv5659
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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