A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326167



Internal ID20859301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69060198..69060677hg38UCSC Ensembl
chr1:69525881..69526360hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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