A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504231



Internal ID22562174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9404663..9458818hg38UCSC Ensembl
chr7:9444293..9498448hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3854156
hg1954156
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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