A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149693



Internal ID20716733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8789506..8971020hg38UCSC Ensembl
chr6:8789739..8971253hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38181515
hg19181515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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