A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143743



Internal ID21420551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78728524..78728863hg38UCSC Ensembl
chr7:78357840..78358179hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570268
Supporting Variants
SamplesHG00731
Known GenesMAGI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143743
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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