A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662044



Internal ID21610349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91571765..91571765hg38UCSC Ensembl
chr13:92224019..92224019hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096064
SamplesNA19238
Known GenesGPC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662044
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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