A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004592



Internal ID20571632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78616435..78627973hg38UCSC Ensembl
chr12:79010215..79021753hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3811539
hg1911539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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