A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325452



Internal ID20858583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111220105..111275674hg38UCSC Ensembl
chr1:111762727..111818296hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3855570
hg1955570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050897
Samples
Known GenesCHI3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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