A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480604



Internal ID22538507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16122949..16128517hg38UCSC Ensembl
chr2:16263071..16268639hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480604
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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