A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060382



Internal ID19149601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12337746..12418865hg38UCSC Ensembl
Innerchr17:12241063..12322182hg19UCSC Ensembl
Innerchr17:12181788..12262907hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3881120
hg1981120
hg1881120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560352
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060382
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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