A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167561



Internal ID20734601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50535601..50546300hg38UCSC Ensembl
chr8:51448161..51458860hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422891
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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