A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741008



Internal ID20516985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064876..72065181hg38UCSC Ensembl
chr10:73824634..73824939hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262171
Samples
Known GenesSPOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741008
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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