A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318049



Internal ID20851140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172076578..172077098hg38UCSC Ensembl
chr1:172045718..172046238hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053872
Samples
Known GenesDNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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