A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610707



Internal ID20983778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132483276..132483995hg38UCSC Ensembl
chr6:132804415..132805134hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139724
Samples
Known GenesSTX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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