A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320089



Internal ID20853187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6297292..6298389hg38UCSC Ensembl
chr1:6357352..6358449hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062254
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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