A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369953



Internal ID22595622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56621860..56621860hg38UCSC Ensembl
chr17:54699221..54699221hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369953
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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