A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327952



Internal ID20861096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185291306..185293219hg38UCSC Ensembl
chr1:185260438..185262351hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054477
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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