A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400872



Internal ID22458742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214864037..214866106hg38UCSC Ensembl
chr2:215728761..215730830hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382070
hg192070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400872
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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