A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169111



Internal ID20736151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55170085..55170535hg38UCSC Ensembl
chr8:56082645..56083095hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429272
Supporting Variants
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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