A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481976



Internal ID22539881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201199842..201212125hg38UCSC Ensembl
chr2:202064565..202076848hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3812284
hg1912284
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832415
Supporting Variants
Samples
Known GenesCASP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481976
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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