A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349371



Internal ID21006924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100577491..100579859hg38UCSC Ensembl
chr2:101193953..101196321hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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