A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326163



Internal ID20859297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235187184..235191351hg38UCSC Ensembl
chr1:235350499..235354666hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg384168
hg194168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202415
Samples
Known GenesARID4B, MIR4753
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326163
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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