A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325908



Internal ID20859041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205939544..205941610hg38UCSC Ensembl
chr1:205908672..205910738hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057068
Samples
Known GenesSLC26A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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