A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439772



Internal ID21097325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73909571..73919230hg38UCSC Ensembl
chr9:76524487..76534146hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389660
hg199660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184294
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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