A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061524



Internal ID19150743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83046425..83091923hg38UCSC Ensembl
Innerchr17:81004301..81049725hg19UCSC Ensembl
Innerchr17:78597590..78643088hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3845499
hg1945425
hg1845499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3569019
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)nsv1061524
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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