A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928



Internal ID15550786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:120345994..120377889hg38UCSC Ensembl
Outerchr7:119986048..120017943hg19UCSC Ensembl
Outerchr7:119773284..119805179hg18UCSC Ensembl
Outerchr7:119579999..119611894hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg389093
hg199093
hg189093
hg179093
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681
SamplesNA19240
Known GenesKCND2
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)nsv5928
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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