A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006121



Internal ID20573161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98004874..98134562hg38UCSC Ensembl
chr12:98398652..98528340hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38129689
hg19129689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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