A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025311



Internal ID21934654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5932176..5932242hg38UCSC Ensembl
chr12:6041342..6041408hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613748
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025311
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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