A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421772



Internal ID21079325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149716014..149719262hg38UCSC Ensembl
chr7:149413105..149416353hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383249
hg193249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154053
Samples
Known GenesKRBA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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