A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488223



Internal ID22546140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158710143..158713942hg38UCSC Ensembl
chr2:159566655..159570454hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488223
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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