A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439103



Internal ID21096656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72571055..72579960hg38UCSC Ensembl
chr9:75185971..75194876hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388906
hg198906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180437
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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