A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057362



Internal ID20624402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210494730..210505546hg38UCSC Ensembl
chr1:210668074..210678890hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3810817
hg1910817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322758
Supporting Variants
Samples
Known GenesHHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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