A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504846



Internal ID22562790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28024714..28031113hg38UCSC Ensembl
chr7:28064333..28070732hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846213
Supporting Variants
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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