A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705494



Internal ID15442146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66275878..66328575hg38UCSC Ensembl
Innerchr3:66326302..66378999hg19UCSC Ensembl
Innerchr3:66408992..66461689hg18UCSC Ensembl
Innerchr3:66408992..66461689hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3852698
hg1952698
hg1852698
hg1752698
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528820
Supporting Variants
Samples
Known GenesSLC25A26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705494
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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