A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903518



Internal ID22678686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104282244..104282399hg38UCSC Ensembl
chr6:104730119..104730274hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903518
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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