A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328769



Internal ID20861919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55319417..55330313hg38UCSC Ensembl
chr1:55785090..55795986hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3810897
hg1910897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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