A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438661



Internal ID21096214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95292201..95292700hg38UCSC Ensembl
chr9:98054483..98054982hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180045
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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