A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002086



Internal ID20569126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:59153258..59263548hg38UCSC Ensembl
chr12:59547039..59657329hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38110291
hg19110291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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