A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330263



Internal ID20863419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9965129..9968579hg38UCSC Ensembl
chr1:10025187..10028637hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383451
hg193451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066188
Samples
Known GenesNMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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