A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071062



Internal ID21471786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58621956..58621956hg38UCSC Ensembl
chr10:60381716..60381716hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640058
Supporting Variants
SamplesHG03125
Known GenesBICC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071062
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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