A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325672



Internal ID20858803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92849406..92849999hg38UCSC Ensembl
chr1:93314963..93315556hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065215
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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