A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880056



Internal ID22655026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111195040..111530461hg38UCSC Ensembl
chr1:111737662..112073083hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38335422
hg19335422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356798
Samples
Known GenesADORA3, ATP5F1, C1orf162, CHI3L2, CHIA, CHIAP2, DENND2D, OVGP1, PGCP1, PIFO, WDR77
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880056
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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