A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927536



Internal ID22702764
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 Variantsnssv17359128
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927536
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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