A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431414



Internal ID21088967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72115179..72119567hg38UCSC Ensembl
chr8:73027414..73031802hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg384389
hg194389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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