A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488658



Internal ID265961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7260124..7367856hg38UCSC Ensembl
chr10:7302086..7409818hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38107733
hg19107733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030595
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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