A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332028



Internal ID20865197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101102198..101102651hg38UCSC Ensembl
chr1:101567754..101568207hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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