A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331758



Internal ID20864925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54986637..54986872hg38UCSC Ensembl
chr1:55452310..55452545hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062199
Samples
Known GenesTMEM61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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