A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485032



Internal ID22542943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112623845..112624944hg38UCSC Ensembl
chr2:113381422..113382521hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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