A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632513



Internal ID21580818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132864618..132864618hg38UCSC Ensembl
chr5:132200310..132200310hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137494
SamplesHG01505
Known GenesGDF9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632513
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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