A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997223



Internal ID20564263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118064797..118065503hg38UCSC Ensembl
chr12:118502602..118503308hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493163
Supporting Variants
Samples
Known GenesVSIG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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