A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233969



Internal ID20801010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14634490..14763616hg38UCSC Ensembl
chr7:14674115..14803241hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38129127
hg19129127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617594
Supporting Variants
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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