A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907817



Internal ID22683027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2559241..2559489hg38UCSC Ensembl
chr7:2598875..2599123hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429946
Samples
Known GenesIQCE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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