A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072820



Internal ID21982053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37117861..37117861hg38UCSC Ensembl
chr6:37085637..37085637hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072820
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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