A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219716



Internal ID20786756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64593536..64719409hg38UCSC Ensembl
chr7:64053914..64179787hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38125874
hg19125874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617910
Supporting Variants
Samples
Known GenesLOC100128885, MIR6839, ZNF107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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