A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375788



Internal ID22601457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57154194..57154284hg38UCSC Ensembl
chr17:55231555..55231645hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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