A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603590



Internal ID20976661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147002834..147013422hg38UCSC Ensembl
chr6:147323970..147334558hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3810589
hg1910589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139087
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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