A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405896



Internal ID21063449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89297817..89313800hg38UCSC Ensembl
chr6:90007536..90023519hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3815984
hg1915984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148095
Samples
Known GenesGABRR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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