A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327916



Internal ID20861060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178653440..178663054hg38UCSC Ensembl
chr1:178622575..178632189hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg389615
hg199615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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