A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316182



Internal ID20849260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154312870..154322011hg38UCSC Ensembl
chr1:154285346..154294487hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389142
hg199142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052021
Samples
Known GenesAQP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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