A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071849



Internal ID21504880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74139370..74141203hg38UCSC Ensembl
chr10:75899128..75900961hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381834
hg191834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599094
Supporting Variants
SamplesNA19650
Known GenesAP3M1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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