A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060750



Internal ID20627790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40333700..40342211hg38UCSC Ensembl
chr1:40799372..40807883hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg388512
hg198512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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