A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7054n223



Internal ID22810022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111225733..111555583hg38UCSC Ensembl
chr7:110865789..111195639hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38329851
hg19329851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6611151, nsv6616374, nsv6614176
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7054n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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