A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061665



Internal ID19150884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83017872..83091923hg38UCSC Ensembl
Innerchr17:80975748..81049725hg19UCSC Ensembl
Innerchr17:78569037..78643088hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3874052
hg1973978
hg1874052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3299n100
Supporting Variantsnssv3567910
Samples
Known GenesB3GNTL1, METRNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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