A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001846



Internal ID20568886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56439107..56443347hg38UCSC Ensembl
chr12:56832891..56837131hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg384241
hg194241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465427
Supporting Variants
Samples
Known GenesTIMELESS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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