A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003866



Internal ID70207
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 StatusS
Merged Variantsnsv5483538
Supporting Variants
Samples
Known GenesFAM115C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003866
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00203


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