A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502809



Internal ID22560750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75415882..75427168hg38UCSC Ensembl
chr7:75045160..75056450hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3811287
hg1911291
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863878
Supporting Variants
Samples
Known GenesNSUN5P1, POM121C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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