A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925482



Internal ID21345553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55237642..55237707hg38UCSC Ensembl
chr7:55305335..55305400hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198349
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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