A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495075



Internal ID22553007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181222027..181225926hg38UCSC Ensembl
chr5:180649027..180652926hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842523
Supporting Variants
Samples
Known GenesMIR4638, TRIM41
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495075
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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