A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071164



Internal ID21454777
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 StatusS
Merged Variantsnsv5629682
Supporting Variants
SamplesHG02011
Known GenesFAM13C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071164
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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