A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598747



Internal ID21547375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918724..70918878hg38UCSC Ensembl
chr10:72678481..72678635hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071807
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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