A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625043



Internal ID21573348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45083586..45083586hg38UCSC Ensembl
chr7:45123185..45123185hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157810
SamplesHG02011
Known GenesNACAD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625043
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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