A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353573



Internal ID21011126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13923837..13948095hg38UCSC Ensembl
chr2:14063962..14088220hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3824259
hg1924259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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