A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484794



Internal ID22542703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3725995..3764133hg38UCSC Ensembl
chr2:3773585..3811723hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3838139
hg1938139
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484794
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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