A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705468



Internal ID15095434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247686171..247762088hg38UCSC Ensembl
Innerchr1:247849473..247925390hg19UCSC Ensembl
Innerchr1:245916096..245992013hg18UCSC Ensembl
Innerchr1:244175514..244251431hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3875918
hg1975918
hg1875918
hg1775918
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515858
Supporting Variants
Samples
Known GenesOR1C1, OR6F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705468
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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