A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320350



Internal ID20853448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169710301..169711100hg38UCSC Ensembl
chr1:169679442..169680241hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053323
Samples
Known GenesSELL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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