A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445287



Internal ID21102840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81644735..81645101hg38UCSC Ensembl
chr9:84259650..84260016hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192303
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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