A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494541



Internal ID22552472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40542697..40558197hg38UCSC Ensembl
chr4:40544714..40560214hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3815501
hg1915501
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839619
Supporting Variants
Samples
Known GenesRBM47
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494541
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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