A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325666



Internal ID20858797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158677195..158678014hg38UCSC Ensembl
chr1:158646985..158647804hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053447
Samples
Known GenesSPTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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