A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617594



Internal ID20990665
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 StatusM
Merged Variants
Supporting Variantsnssv18233969
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617594
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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