A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001790



Internal ID21911133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2324959..2325420hg38UCSC Ensembl
chr6:2325193..2325654hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575815
Samples
Known GenesGMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001790
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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