A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486283



Internal ID22544197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127462666..127464865hg38UCSC Ensembl
chr2:128220242..128222441hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830952
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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