A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333894



Internal ID20867075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55976101..55981800hg38UCSC Ensembl
chr1:56441774..56447473hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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