A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6732



Internal ID15551671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130135781..130180043hg38UCSC Ensembl
Outerchr9:132898060..132942322hg19UCSC Ensembl
Outerchr9:131937881..131982143hg18UCSC Ensembl
Outerchr9:129977614..130021876hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3844263
hg1944263
hg1844263
hg1744263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1802
SamplesNA18555
Known GenesGPR107, NCS1
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)nsv6732
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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