A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893778



Internal ID22668843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10928185..10928239hg38UCSC Ensembl
chr6:10928418..10928472hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422575
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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