A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611019



Internal ID20984090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114759056..114759770hg38UCSC Ensembl
chr7:114399111..114399825hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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