A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895051



Internal ID22670128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126594610..126609783hg38UCSC Ensembl
chr6:126915756..126930929hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3815174
hg1915174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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