A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642886



Internal ID21591191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30471102..30471102hg38UCSC Ensembl
chr7:30510718..30510718hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144361
SamplesHG02587
Known GenesNOD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642886
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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