A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062630



Internal ID20629670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66792266..66798322hg38UCSC Ensembl
chr1:67257949..67264005hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg386057
hg196057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330049
Supporting Variants
Samples
Known GenesINSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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