A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371410



Internal ID21028963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84788065..84893648hg38UCSC Ensembl
chr3:84837216..84942799hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38105584
hg19105584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104125
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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