A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940035



Internal ID22715438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51433531..51457626hg38UCSC Ensembl
chr17:49510892..49534987hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3824096
hg1924096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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