A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333623



Internal ID20866803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167224857..167236132hg38UCSC Ensembl
chr1:167194094..167205369hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201528
Samples
Known GenesPOU2F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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