A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000329



Internal ID20567369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39449656..39518736hg38UCSC Ensembl
chr12:39843458..39912538hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3869081
hg1969081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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