A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328012



Internal ID20861156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244936534..244958894hg38UCSC Ensembl
chr1:245099836..245122196hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3822361
hg1922361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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