A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603581



Internal ID21795628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42228030..42228492hg38UCSC Ensembl
chr12:42621832..42622294hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021898
Supporting Variants
Samples
Known GenesYAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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