A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497247



Internal ID22555181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76721037..76722920hg38UCSC Ensembl
chr4:77642190..77644073hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840390
Supporting Variants
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497247
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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