A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3107n100



Internal ID19013475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15703953..16150198hg38UCSC Ensembl
chr17:15607267..16053512hg19UCSC Ensembl
chr17:15547992..15994237hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38446246
hg19446246
hg18446246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066023, nsv1061222
Samples
Known GenesADORA2B, CDRT15P2, MEIS3P1, NCOR1, TBC1D26, TTC19, ZNF286A, ZSWIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3107n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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