A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7056n223



Internal ID22810024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111266147..111686617hg38UCSC Ensembl
chr7:110906203..111326673hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38420471
hg19420471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6610966, nsv6617397, nsv6607452, nsv6615425, nsv6606407, nsv6608158, nsv6616239
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7056n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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