A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096357



Internal ID20663397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150002806..150003251hg38UCSC Ensembl
chr3:149720593..149721038hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372730
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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