A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224486



Internal ID20791526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87641331..87642102hg38UCSC Ensembl
chr6:88351049..88351820hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410217
Supporting Variants
Samples
Known GenesORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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