A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639077



Internal ID21587382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60244451..60244451hg38UCSC Ensembl
chr10:62004209..62004209hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071203
SamplesHG01114
Known GenesANK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639077
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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