A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451836



Internal ID21109389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92617509..92617562hg38UCSC Ensembl
chr9:95379791..95379844hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192542
Samples
Known GenesIPPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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