A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120905



Internal ID20687945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73492466..73500112hg38UCSC Ensembl
chr4:74358183..74365829hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg387647
hg197647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378672
Supporting Variants
Samples
Known GenesAFM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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