A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419836



Internal ID21077389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155207659..155207902hg38UCSC Ensembl
chr7:154999369..154999612hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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