A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453870



Internal ID21111423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125491264..125503074hg38UCSC Ensembl
chr9:128253543..128265353hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811811
hg1911811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176688
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453870
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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