A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461858



Internal ID22519744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31764086..31772548hg38UCSC Ensembl
chr10:32053014..32061476hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388463
hg198463
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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