A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603906



Internal ID21795953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49135595..49135970hg38UCSC Ensembl
chr12:49529378..49529753hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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