A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327586



Internal ID20860726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235983140..236093515hg38UCSC Ensembl
chr1:236146440..236256815hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38110376
hg19110376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201875
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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