A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155429



Internal ID20722469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4743938..4751018hg38UCSC Ensembl
chr7:4783569..4790649hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg387081
hg197081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614459
Supporting Variants
Samples
Known GenesFOXK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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