A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3298n100



Internal ID20154914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82955017..83091923hg38UCSC Ensembl
chr17:80912893..81049725hg19UCSC Ensembl
chr17:78506182..78643088hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38136907
hg19136833
hg18136907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059548, nsv1057407, nsv1057542, nsv1060098
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)dgv3298n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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