A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318699



Internal ID20851791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226025996..226027373hg38UCSC Ensembl
chr1:226213697..226215074hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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