A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030761



Internal ID21940104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2008327..2008382hg38UCSC Ensembl
chr12:2117493..2117548hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030761
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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