A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600974



Internal ID21793021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95344317..95344609hg38UCSC Ensembl
chr12:95738093..95738385hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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