A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635099



Internal ID21583404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132698175..132698175hg38UCSC Ensembl
chr7:132382934..132382934hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145940
SamplesHG00731
Known GenesFLJ40288
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635099
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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