A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002039



Internal ID21911382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42160965..42162190hg38UCSC Ensembl
chr6:42128703..42129928hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574467
Samples
Known GenesGUCA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002039
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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