A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064966



Internal ID19154185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20527855..20705958hg38UCSC Ensembl
Innerchr17:20431168..20609271hg19UCSC Ensembl
Innerchr17:20371760..20549863hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38178104
hg19178104
hg18178104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3121n100
Supporting Variantsnssv3560914
Samples
Known GenesCDRT15L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064966
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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