A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110172



Internal ID20677212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139214901..139222219hg38UCSC Ensembl
chr4:140136055..140143373hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387319
hg197319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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