A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331189



Internal ID20864351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52132345..52136719hg38UCSC Ensembl
chr1:52598017..52602391hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384375
hg194375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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