A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508982



Internal ID20882287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8925194..8925542hg38UCSC Ensembl
chr17:8828511..8828859hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039094
Samples
Known GenesPIK3R5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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