A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427372



Internal ID21084925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19147675..19222070hg38UCSC Ensembl
chr9:19147673..19222068hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3874396
hg1974396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7636n223
Supporting Variantsnssv18175544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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