A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408457



Internal ID22466327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175841611..175841666hg38UCSC Ensembl
chr2:176706339..176706394hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408457
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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