A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485895



Internal ID22543808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12569685..12572638hg38UCSC Ensembl
chr2:12709811..12712764hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485895
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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