A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003722



Internal ID21913065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107034873..107034933hg38UCSC Ensembl
chr6:107356077..107356137hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558751
Samples
Known GenesC6orf203
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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