A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345945



Internal ID21003498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84319101..84336600hg38UCSC Ensembl
chr2:84546225..84563724hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3817500
hg1917500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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