A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422187



Internal ID21079740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138597353..138607475hg38UCSC Ensembl
chr7:138282098..138292220hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810123
hg1910123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155217
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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