A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611184



Internal ID20984255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76175349..76179206hg38UCSC Ensembl
chr7:75804667..75808524hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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