A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021836



Internal ID21931179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6568670..6568960hg38UCSC Ensembl
chr12:6677836..6678126hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021836
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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