A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143447



Internal ID21420429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27743756..27744103hg38UCSC Ensembl
chr7:27783375..27783722hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580573
Supporting Variants
SamplesHG00731
Known GenesTAX1BP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143447
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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