A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968



Internal ID15204144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138579315..138614193hg38UCSC Ensembl
Outerchr7:138264060..138298938hg19UCSC Ensembl
Outerchr7:137914600..137949478hg18UCSC Ensembl
Outerchr7:137721315..137756193hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384867
hg194867
hg184867
hg174867
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583
SamplesNA12878
Known GenesSVOPL, TRIM24
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)nsv5968
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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