A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334579



Internal ID20867766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178924118..178928726hg38UCSC Ensembl
chr1:178893253..178897861hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg384609
hg194609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv451n223
Supporting Variantsnssv18054099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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