A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069169



Internal ID21457636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14014954..14015272hg38UCSC Ensembl
chr10:14056953..14057271hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590172
Supporting Variants
SamplesHG02587
Known GenesFRMD4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069169
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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