A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv882n209



Internal ID22826957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15750946..16863323hg38UCSC Ensembl
chr17:15654260..16766637hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381112378
hg191112378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5943631, nsv5940764, nsv5945891
Samples
Known GenesADORA2B, CCDC144A, CDRT15P2, CENPV, FAM106CP, FAM211A, FAM211A-AS1, KRT16P2, MEIS3P1, MIR1288, NCOR1, PIGL, SNORD49A, SNORD49B, SNORD65, TRPV2, TTC19, UBB, USP32P1, ZNF287, ZNF624, ZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv882n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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