A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14241158



Internal ID21308920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248585893..248632551hg38UCSC Ensembl
Outerchr1:248574146..248633821hg38UCSC Ensembl
Innerchr1:248749194..248795852hg19UCSC Ensembl
Outerchr1:248737447..248797122hg19UCSC Ensembl
Innerchr1:246815817..246862475hg18UCSC Ensembl
Outerchr1:246804070..246863745hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3859676
hg1959676
hg1859676
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169954
Supporting Variants
SamplesNGO_46
Known GenesOR2T10, OR2T11, OR2T34
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14241158
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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