A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329283



Internal ID20862434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151318440..151321601hg38UCSC Ensembl
chr1:151290916..151294077hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383162
hg193162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200413
Samples
Known GenesPI4KB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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