A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449649



Internal ID21107202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131792704..131795719hg38UCSC Ensembl
chr9:134668091..134671106hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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