A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6702



Internal ID15204952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:122151820..122184094hg38UCSC Ensembl
Outerchr9:124914099..124946373hg19UCSC Ensembl
Outerchr9:123953920..123986194hg18UCSC Ensembl
Outerchr9:121993653..122025927hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387162
hg197162
hg187162
hg177162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6295
SamplesNA12156
Known GenesMORN5, NDUFA8
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)nsv6702
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