A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377155



Internal ID22435025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38639890..38641115hg38UCSC Ensembl
chr17:36796143..36797368hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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