A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619059



Internal ID20992130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95604702..95618975hg38UCSC Ensembl
chr7:95234014..95248287hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3814274
hg1914274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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