A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486973



Internal ID22544888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57757717..57767152hg38UCSC Ensembl
chr2:57984852..57994287hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg389436
hg199436
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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