A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030244



Internal ID21939587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67767249..67771909hg38UCSC Ensembl
chr12:68161029..68165689hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg384661
hg194661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030244
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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