A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141794



Internal ID20708834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37220758..37222231hg38UCSC Ensembl
chr6:37188534..37190007hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg381474
hg191474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410844
Supporting Variants
Samples
Known GenesTMEM217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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