A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488153



Internal ID22546070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84940466..84943765hg38UCSC Ensembl
chr2:85167590..85170889hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488153
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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