A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323868



Internal ID20856991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154215109..154216052hg38UCSC Ensembl
chr1:154187585..154188528hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052016
Samples
Known GenesC1orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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