A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319669



Internal ID20852764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36731840..36733067hg38UCSC Ensembl
chr1:37197441..37198668hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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