A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602137



Internal ID21550792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73690257..73690628hg38UCSC Ensembl
chr10:75450015..75450386hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071630
SamplesNA19983
Known GenesAGAP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602137
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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