A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624702



Internal ID21573007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118443247..118443247hg38UCSC Ensembl
chr7:118083301..118083301hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153293
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624702
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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