A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054372



Internal ID20621413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182705544..182705725hg38UCSC Ensembl
chr1:182674679..182674860hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.04647


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