A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335523



Internal ID20868716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25612831..25614227hg38UCSC Ensembl
chr1:25939322..25940718hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335523
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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