A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019896



Internal ID21929239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2041295..2044263hg38UCSC Ensembl
chr6:2041529..2044497hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567256
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019896
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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