A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326754



Internal ID20859891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168106386..168119506hg38UCSC Ensembl
chr1:168075624..168088744hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3813121
hg1913121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201534
Samples
Known GenesGPR161
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326754
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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