A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997817



Internal ID20564857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121920821..121921138hg38UCSC Ensembl
chr12:122358727..122359044hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478832
Supporting Variants
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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