A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318295



Internal ID20851387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206038769..206041226hg38UCSC Ensembl
chr1:206300142..206302599hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382458
hg192458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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