A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483538



Internal ID260974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143725804..143744402hg38UCSC Ensembl
chr7:143422897..143441495hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3818599
hg1918599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003866
Samples
Known GenesFAM115C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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