A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316859



Internal ID20849941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105750499..105788056hg38UCSC Ensembl
chr1:106293121..106330678hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3837558
hg1937558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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