A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322766



Internal ID20855880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229583001..229587700hg38UCSC Ensembl
chr1:229718748..229723447hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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