A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6773



Internal ID15205030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137693762..137746094hg38UCSC Ensembl
Outerchr9:140588214..140640546hg19UCSC Ensembl
Outerchr9:139708035..139760367hg18UCSC Ensembl
Outerchr9:137864051..137916383hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385791
hg195791
hg185791
hg175791
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5195, nssv2824, nssv845, nssv8678, nssv3761, nssv9476
SamplesNA18517, NA19129, NA12156, NA12878, NA19240, NA18555
Known GenesEHMT1
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)nsv6773
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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