A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438074



Internal ID21095627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68835338..68837966hg38UCSC Ensembl
chr9:71450254..71452882hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382629
hg192629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187458
Samples
Known GenesPIP5K1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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