A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315966



Internal ID20849042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60447956..60448310hg38UCSC Ensembl
chr1:60913628..60913982hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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