A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608863



Internal ID20981934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14122235..14222280hg38UCSC Ensembl
chr7:14161860..14261905hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38100046
hg19100046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222159
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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