A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332858



Internal ID20866033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87203101..87208536hg38UCSC Ensembl
chr1:87668784..87674219hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg385436
hg195436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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