A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064764



Internal ID20631804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84634927..84635488hg38UCSC Ensembl
chr1:85100610..85101171hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321437
Supporting Variants
Samples
Known GenesC1orf180
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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