A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260764



Internal ID20469982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32061591..32061652hg38UCSC Ensembl
chr12:32214525..32214586hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260764
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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