A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000069



Internal ID20567109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27080366..27086196hg38UCSC Ensembl
chr12:27233299..27239129hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg385831
hg195831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458417
Supporting Variants
Samples
Known GenesC12orf71
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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