A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329771



Internal ID20862924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90794222..90795077hg38UCSC Ensembl
chr1:91259779..91260634hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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