A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920656



Internal ID22695879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102736799..103001222hg38UCSC Ensembl
chr7:102377246..102641669hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38264424
hg19264424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449246
Samples
Known GenesFAM185A, FBXL13, LRRC17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920656
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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