A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325144



Internal ID20858274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235974998..235996594hg38UCSC Ensembl
chr1:236138298..236159894hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3821597
hg1921597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201874
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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