A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015913



Internal ID21925256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31984691..32023790hg38UCSC Ensembl
chr6:31952468..31991567hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3839100
hg1939100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569491
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015913
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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