A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487648



Internal ID22545564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68829454..68838026hg38UCSC Ensembl
chr2:69056586..69065158hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg388573
hg198573
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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