A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606370



Internal ID20979441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147309362..147310092hg38UCSC Ensembl
chr6:147630498..147631228hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141151
Samples
Known GenesSTXBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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