A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438862



Internal ID21096415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116340232..116556451hg38UCSC Ensembl
chr9:119102511..119318730hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38216220
hg19216220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174115
Samples
Known GenesASTN2, LOC100128505, PAPPA, PAPPA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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