A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629682



Internal ID21577987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59315495..59315495hg38UCSC Ensembl
chr10:61075255..61075255hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071164
SamplesHG02011
Known GenesFAM13C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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