A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439721



Internal ID21097274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94185906..94207031hg38UCSC Ensembl
chr9:96948188..96969313hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3821126
hg1921126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191113
Samples
Known GenesMIRLET7DHG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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