A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439936



Internal ID21097489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99906401..99906900hg38UCSC Ensembl
chr9:102668683..102669182hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196408
Samples
Known GenesLOC441461, STX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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