A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452735



Internal ID21110288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126575676..126579687hg38UCSC Ensembl
chr9:129337955..129341966hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384012
hg194012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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