A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001047



Internal ID20568087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47826080..47827960hg38UCSC Ensembl
chr12:48219863..48221743hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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