A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604509



Internal ID21553179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130197470..130197521hg38UCSC Ensembl
chr10:131995734..131995785hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068900
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604509
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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