A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927477



Internal ID22702705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20336510..20337487hg38UCSC Ensembl
chr7:20376133..20377110hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443174
Samples
Known GenesITGB8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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