A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320682



Internal ID20853783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152155419..152155894hg38UCSC Ensembl
chr1:152127895..152128370hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052321
Samples
Known GenesRPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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