A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404192



Internal ID22462062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88832767..89176324hg38UCSC Ensembl
chr2:89132280..89475808hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38343558
hg19343529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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