A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317091



Internal ID20850175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151302501..151303196hg38UCSC Ensembl
chr1:151274977..151275672hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051321
Samples
Known GenesPI4KB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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