A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860977



Internal ID22635912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91977197..92001222hg38UCSC Ensembl
chr13:92629451..92653475hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3824026
hg1924025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456544
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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