A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409789



Internal ID22467659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123052736..123053071hg38UCSC Ensembl
chr6:123373881..123374216hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905537
Supporting Variants
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409789
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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