A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323728



Internal ID20856849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55236012..55239309hg38UCSC Ensembl
chr1:55701685..55704982hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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