A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002331



Internal ID20569371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64808964..64810290hg38UCSC Ensembl
chr12:65202744..65204070hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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