A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602685



Internal ID21551344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2231845..2232348hg38UCSC Ensembl
chr10:2274039..2274542hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069708
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602685
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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