A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368983



Internal ID21026536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72615193..72616764hg38UCSC Ensembl
chr3:72664344..72665915hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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