A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018334



Internal ID21927677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40601487..40601559hg38UCSC Ensembl
chr8:40459006..40459078hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577553
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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