A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459668



Internal ID22517554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87611460..87619979hg38UCSC Ensembl
chr13:88263715..88272234hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg388520
hg198520
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849613
Supporting Variants
Samples
Known GenesMIR4500, MIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459668
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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