A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607846



Internal ID20980917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147219401..147221600hg38UCSC Ensembl
chr6:147540537..147542736hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141140
Samples
Known GenesSTXBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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