A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004249



Internal ID21913592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123189519..123189637hg38UCSC Ensembl
chr10:124949035..124949153hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004249
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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