A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140753



Internal ID20707793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26464534..26465845hg38UCSC Ensembl
chr6:26464762..26466073hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414749
Supporting Variants
Samples
Known GenesBTN2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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