A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169304



Internal ID20736344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64783154..64783778hg38UCSC Ensembl
chr8:65695711..65696335hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431601
Supporting Variants
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00071


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