A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065162



Internal ID19154381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:828833..907902hg38UCSC Ensembl
Innerchr17:732073..811142hg19UCSC Ensembl
Innerchr17:678823..757892hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3879070
hg1979070
hg1879070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3076n100
Supporting Variantsnssv3560053
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065162
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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