A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318268



Internal ID20851360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150877952..150879766hg38UCSC Ensembl
chr1:150850428..150852242hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381815
hg191815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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