A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498176



Internal ID22556111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108530219..108538488hg38UCSC Ensembl
chr4:109451375..109459644hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388270
hg198270
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837285
Supporting Variants
Samples
Known GenesRPL34-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498176
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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