A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456884



Internal ID22514764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68865889..68905360hg38UCSC Ensembl
chr13:69440021..69479492hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3839472
hg1939472
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853537
Supporting Variants
Samples
Known GenesLINC00550
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456884
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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