A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936768



Internal ID22712127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45360599..45364316hg38UCSC Ensembl
chr17:43437965..43441682hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383718
hg193718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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