A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060098



Internal ID18802629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82955017..83071702hg38UCSC Ensembl
Innerchr17:80912893..81029578hg19UCSC Ensembl
Innerchr17:78506182..78622867hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38116686
hg19116686
hg18116686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3298n100
Supporting Variantsnssv3567906
Samples
Known GenesB3GNTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060098
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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