A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007633



Internal ID21916976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36687581..36691446hg38UCSC Ensembl
chr6:36655358..36659223hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg383866
hg193866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007633
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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