A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619051



Internal ID20992122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114945220..114945632hg38UCSC Ensembl
chr7:114585275..114585687hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149931
Samples
Known GenesMDFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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