A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997229



Internal ID20564269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118097661..118104698hg38UCSC Ensembl
chr12:118535466..118542503hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg387038
hg197038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485295
Supporting Variants
Samples
Known GenesVSIG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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