A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065590



Internal ID20632630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93870201..93872700hg38UCSC Ensembl
chr1:94335757..94338256hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321348
Supporting Variants
Samples
Known GenesDNTTIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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