A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446641



Internal ID21104194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120577339..120578174hg38UCSC Ensembl
chr9:123339617..123340452hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174857
Samples
Known GenesCDK5RAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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