A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945891



Internal ID22721373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15750946..16668217hg38UCSC Ensembl
chr17:15654260..16571531hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38917272
hg19917272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv882n209
Supporting Variantsnssv17379700
Samples
Known GenesADORA2B, CDRT15P2, CENPV, FAM211A, FAM211A-AS1, MEIS3P1, MIR1288, NCOR1, PIGL, SNORD49A, SNORD49B, SNORD65, TRPV2, TTC19, UBB, ZNF287, ZNF624, ZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945891
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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