A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6769



Internal ID15551711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136724467..136752174hg38UCSC Ensembl
Outerchr9:139618919..139646626hg19UCSC Ensembl
Outerchr9:138738740..138766447hg18UCSC Ensembl
Outerchr9:136894756..136922463hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821658
hg1921658
hg1821658
hg1721658
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5192, nssv6303, nssv10692, nssv843
SamplesNA12156, NA18956, NA19240, NA19129
Known GenesFAM69B, LCN10, LCN6, LOC100128593, MIR6722, SNHG7, SNORA17, SNORA43
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)nsv6769
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer