A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328088



Internal ID20861233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66759864..66765045hg38UCSC Ensembl
chr1:67225547..67230728hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385182
hg195182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062627
Samples
Known GenesTCTEX1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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