A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325299



Internal ID20858430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151018956..151021286hg38UCSC Ensembl
chr1:150991432..150993762hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382331
hg192331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053008
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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