A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332691



Internal ID20865865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244041295..244045368hg38UCSC Ensembl
chr1:244204597..244208670hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059612
Samples
Known GenesLOC339529
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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