A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030405



Internal ID87978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16412164..16419683hg38UCSC Ensembl
chr10:16454163..16461682hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387520
hg197520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030405
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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