A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357162



Internal ID21014715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28499739..28559179hg38UCSC Ensembl
chr3:28541230..28600670hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3859441
hg1959441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101342
Samples
Known GenesZCWPW2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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