A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169463



Internal ID20736503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64704277..64705038hg38UCSC Ensembl
chr8:65616834..65617595hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426922
Supporting Variants
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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