A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060414



Internal ID20627454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31938744..31945974hg38UCSC Ensembl
chr1:32404345..32411575hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg387231
hg197231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00171


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