A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997766



Internal ID20564806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121522408..121522741hg38UCSC Ensembl
chr12:121960211..121960544hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479088
Supporting Variants
Samples
Known GenesKDM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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