A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608181



Internal ID21800228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30462642..30463350hg38UCSC Ensembl
chr12:30615575..30616283hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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