A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332360



Internal ID20865530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95662601..95663741hg38UCSC Ensembl
chr1:96128157..96129297hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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