A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596420



Internal ID21545028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59697010..59697137hg38UCSC Ensembl
chr10:61456768..61456895hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071175
SamplesHG00731
Known GenesSLC16A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596420
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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