A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432529



Internal ID21090082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17139317..17145009hg38UCSC Ensembl
chr9:17139315..17145007hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg385693
hg195693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174757
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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