A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919250



Internal ID22694472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155414544..155414864hg38UCSC Ensembl
chr7:155207239..155207559hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919250
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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