A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011400



Internal ID21920743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34241095..34241606hg38UCSC Ensembl
chr6:34208872..34209383hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576251
Samples
Known GenesHMGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011400
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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