A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329219



Internal ID20862370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230601317..230608660hg38UCSC Ensembl
chr1:230737063..230744406hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg387344
hg197344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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