A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330763



Internal ID20863921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117784771..117792432hg38UCSC Ensembl
chr1:118327393..118335054hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg387662
hg197662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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