A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504774



Internal ID22562718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2349039..2351624hg38UCSC Ensembl
chr7:2388674..2391259hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382586
hg192586
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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