A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320480



Internal ID20853578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60155674..60156221hg38UCSC Ensembl
chr1:60621346..60621893hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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