A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999007



Internal ID20566047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31620792..31621095hg38UCSC Ensembl
chr12:31773726..31774029hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02937


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