A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440649



Internal ID21098202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130561266..130562203hg38UCSC Ensembl
chr9:133436653..133437590hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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