A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018521



Internal ID21927864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99384862..99384954hg38UCSC Ensembl
chr7:98982485..98982577hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571774
Samples
Known GenesARPC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018521
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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