A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455754



Internal ID22513631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4176487..4179136hg38UCSC Ensembl
chr10:4218679..4221328hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455754
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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