A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489306



Internal ID22547225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211177631..211217505hg38UCSC Ensembl
chr2:212042356..212082230hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3839875
hg1939875
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489306
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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