A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323977



Internal ID20857100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86029525..86034783hg38UCSC Ensembl
chr1:86495208..86500466hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065481
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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