A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485396



Internal ID22543307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39639272..39644071hg38UCSC Ensembl
chr2:39866412..39871211hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485396
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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