A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327527



Internal ID20860667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85905307..85905894hg38UCSC Ensembl
chr1:86370990..86371577hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065461
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327527
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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