A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441781



Internal ID21099334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126520103..126528324hg38UCSC Ensembl
chr9:129282382..129290603hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg388222
hg198222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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