A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098677



Internal ID21287467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37901253..38383883hg38UCSC Ensembl
Innerchr17:36260806..36539708hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38482631
hg19278903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112343
Supporting Variants
Samplessample402
Known GenesGPR179, LOC440434, MRPL45, SOCS7, TBC1D3, TBC1D3C, TBC1D3F, TBC1D3H
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098677
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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