A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505476



Internal ID22563420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3139833..3147380hg38UCSC Ensembl
chr7:3179467..3187014hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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