A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332848



Internal ID20866023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116246274..116246961hg38UCSC Ensembl
chr1:116788896..116789583hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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