A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452057



Internal ID22509929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76697075..76706835hg38UCSC Ensembl
chr10:78456833..78466593hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389761
hg199761
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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