A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034887



Internal ID90984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42604677..42829183hg38UCSC Ensembl
chr10:43100125..43324631hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38224507
hg19224507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474690
Supporting Variants
Samples
Known GenesBMS1, ZNF33B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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