A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329622



Internal ID20862775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101222533..101231040hg38UCSC Ensembl
chr1:101688089..101696596hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg388508
hg198508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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