A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067123



Internal ID19156342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15579189..15654414hg38UCSC Ensembl
Innerchr17:15482503..15557728hg19UCSC Ensembl
Innerchr17:15423228..15498453hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3875226
hg1975226
hg1875226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560421
Samples
Known GenesCDRT1, TRIM16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067123
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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