A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329108



Internal ID20862259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151941519..151951833hg38UCSC Ensembl
chr1:151913995..151924309hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3810315
hg1910315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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