A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502618



Internal ID22560559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148747107..148750809hg38UCSC Ensembl
chr7:148444199..148447901hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383703
hg193703
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849442
Supporting Variants
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502618
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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