A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612622



Internal ID20985693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4750226..4750920hg38UCSC Ensembl
chr7:4789857..4790551hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155430
Samples
Known GenesFOXK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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