A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004833



Internal ID21914176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152898377..152910930hg38UCSC Ensembl
chr6:153219512..153232065hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3812554
hg1912554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004833
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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