A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627612



Internal ID21575917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107591641..107591641hg38UCSC Ensembl
chr7:107232086..107232086hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156155
SamplesHG03486
Known GenesBCAP29
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627612
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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