A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595705



Internal ID21544312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19237572..19237664hg38UCSC Ensembl
chr10:19526501..19526593hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069940
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595705
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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