A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456544



Internal ID22514422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91977197..92001222hg38UCSC Ensembl
chr13:92629451..92653475hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3824026
hg1924025
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860977
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456544
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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