A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487589



Internal ID22545505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64067955..64074454hg38UCSC Ensembl
chr2:64295089..64301588hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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