A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6756



Internal ID15551697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135089175..135108803hg38UCSC Ensembl
Outerchr9:137981021..138000649hg19UCSC Ensembl
Outerchr9:137120842..137140470hg18UCSC Ensembl
Outerchr9:135206966..135226594hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386436
hg196436
hg186436
hg176436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842
SamplesNA19240
Known GenesOLFM1
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)nsv6756
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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