A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167532



Internal ID20734572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50365001..50365700hg38UCSC Ensembl
chr8:51277561..51278260hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434791
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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