A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695390



Internal ID15085356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108140278..108161212hg38UCSC Ensembl
Innerchr1:108682900..108703834hg19UCSC Ensembl
Innerchr1:108484423..108505357hg18UCSC Ensembl
Innerchr1:108394942..108415876hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820935
hg1920935
hg1820935
hg1720935
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517978
Supporting Variants
Samples
Known GenesSLC25A24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695390
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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