A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923037



Internal ID22698263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22561413..22570990hg38UCSC Ensembl
chr7:22601032..22610609hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg389578
hg199578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430180
Samples
Known GenesLOC100506178
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923037
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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