A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215512



Internal ID20782552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125836745..125850249hg38UCSC Ensembl
chr6:126157891..126171395hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3813505
hg1913505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602299
Supporting Variants
Samples
Known GenesNCOA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215512
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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