A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739951



Internal ID15687221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248586905..248629067hg38UCSC Ensembl
Innerchr1:248750206..248792368hg19UCSC Ensembl
Innerchr1:246816829..246858991hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3842163
hg1942163
hg1842163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549689
Supporting Variants
Samples
Known GenesOR2T10, OR2T11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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