A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012600



Internal ID21921943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76593447..76593527hg38UCSC Ensembl
chr10:78353205..78353285hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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