A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396057



Internal ID22453927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134073005..134084386hg38UCSC Ensembl
chr2:134830576..134841957hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3811382
hg1911382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396057
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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