A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739734



Internal ID16033690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248177298..248384644hg38UCSC Ensembl
Innerchr1:248340600..248547945hg19UCSC Ensembl
Innerchr1:246407223..246614568hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38207347
hg19207346
hg18207346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549626
Supporting Variants
Samples
Known GenesOR14C36, OR2M2, OR2M3, OR2M4, OR2M7, OR2T12, OR2T33, OR2T4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739734
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