A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015874



Internal ID21925217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111161780..111467134hg38UCSC Ensembl
chr7:110801836..111107190hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38305355
hg19305355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562319
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015874
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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