A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935621



Internal ID22710965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33711739..33715436hg38UCSC Ensembl
chr17:32038758..32042455hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383698
hg193698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380474
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935621
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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