A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324865



Internal ID20857995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186522880..186527405hg38UCSC Ensembl
chr1:186492012..186496537hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg384526
hg194526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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