A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315679



Internal ID20848751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63856301..64041300hg38UCSC Ensembl
chr1:64321972..64506972hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38185000
hg19185001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062333
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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