A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605119



Internal ID20978190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43810722..43811584hg38UCSC Ensembl
chr7:43850321..43851183hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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