A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373089



Internal ID21030642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57286978..57287609hg38UCSC Ensembl
chr3:57321006..57321637hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103501
Samples
Known GenesASB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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