A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315731



Internal ID20848803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44783332..44785657hg38UCSC Ensembl
chr1:45249004..45251329hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382326
hg192326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061415
Samples
Known GenesBEST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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