A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054657



Internal ID20621697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182055954..182071277hg38UCSC Ensembl
chr1:182025089..182040412hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3815324
hg1915324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328679
Supporting Variants
Samples
Known GenesZNF648
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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