A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604432



Internal ID21553101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7358160..7358235hg38UCSC Ensembl
chr10:7400122..7400197hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071398
SamplesNA12878
Known GenesSFMBT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604432
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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