A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038844



Internal ID93646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124546291..124546862hg38UCSC Ensembl
chr10:126234860..126235431hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495374
Supporting Variants
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038844
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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