A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415526



Internal ID22473396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123601914..123602332hg38UCSC Ensembl
chr6:123923059..123923477hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905151
Supporting Variants
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415526
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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