A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067411



Internal ID21486439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1011052..1011137hg38UCSC Ensembl
chr10:1056992..1057077hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594466
Supporting Variants
SamplesNA12878
Known GenesGTPBP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067411
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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