A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329112



Internal ID20862263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92897401..92904000hg38UCSC Ensembl
chr1:93362958..93369557hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065218
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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