A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292067



Internal ID20501285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8006916..8006980hg38UCSC Ensembl
chr12:8159512..8159576hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292067
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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