A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486854



Internal ID22544769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53202314..53216661hg38UCSC Ensembl
chr2:53429452..53443799hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3814348
hg1914348
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833303
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486854
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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