A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492925



Internal ID22550853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139045534..139046633hg38UCSC Ensembl
chr4:139966688..139967787hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838263
Supporting Variants
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492925
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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