A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112356



Internal ID20679396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173352150..173358308hg38UCSC Ensembl
chr4:174273301..174279459hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg386159
hg196159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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