A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456864



Internal ID22514744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51319154..51320553hg38UCSC Ensembl
chr13:51893290..51894689hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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