A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004135



Internal ID20571175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77036585..77040608hg38UCSC Ensembl
chr12:77430365..77434388hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg384024
hg194024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458918
Supporting Variants
Samples
Known GenesE2F7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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