A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7119



Internal ID15190059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:121105502..121138401hg38UCSC Ensembl
Outerchr4:122026657..122059556hg19UCSC Ensembl
Outerchr4:122246107..122279006hg18UCSC Ensembl
Outerchr4:122384262..122417161hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386527
hg196527
hg186527
hg176527
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4492
Supporting Variants
SamplesNA12156
Known GenesTNIP3
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)nssv7119
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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