A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375326



Internal ID21032879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56158244..56169220hg38UCSC Ensembl
chr3:56192272..56203248hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3810977
hg1910977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102814
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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