A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331981



Internal ID20865150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107218338..107225920hg38UCSC Ensembl
chr1:107760960..107768542hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387583
hg197583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051024
Samples
Known GenesNTNG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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