A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062335



Internal ID20629375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63857101..63955800hg38UCSC Ensembl
chr1:64322772..64421471hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3898700
hg1998700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327296
Supporting Variants
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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