A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379052



Internal ID22436922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64218500..64227775hg38UCSC Ensembl
chr17:62295860..62305135hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg389276
hg199276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940880
Supporting Variants
Samples
Known GenesTEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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