A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601768



Internal ID21550418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6000959..6001135hg38UCSC Ensembl
chr10:6042922..6043098hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071190
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601768
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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