A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323211



Internal ID20856327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83636385..83637288hg38UCSC Ensembl
chr1:84102068..84102971hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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