A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14344572



Internal ID22252124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49742433..49742501hg38UCSC Ensembl
chr10:50950479..50950547hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212335
Supporting Variants
SamplesHG00733
Known GenesOGDHL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14344572
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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