A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159540



Internal ID20726580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74489611..74498896hg38UCSC Ensembl
chr7:73903941..73913226hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389286
hg199286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617400
Supporting Variants
Samples
Known GenesGTF2IRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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