A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037914



Internal ID21947257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94482201..94482359hg38UCSC Ensembl
chr12:94875977..94876135hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037914
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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