A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141472



Internal ID340669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22627808..22627881hg38UCSC Ensembl
chr10:22916737..22916810hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032168
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141472
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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