A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649165



Internal ID21597470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92347882..92347882hg38UCSC Ensembl
chr13:93000135..93000135hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084535
SamplesHG00731
Known GenesGPC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649165
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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