A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321687



Internal ID20854795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9954491..9956538hg38UCSC Ensembl
chr1:10014549..10016596hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066183
Samples
Known GenesNMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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