A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904948



Internal ID22680128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26587377..26588829hg38UCSC Ensembl
chr6:26587605..26589057hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904948
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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