A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913755



Internal ID22688971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22713363..22724047hg38UCSC Ensembl
chr10:23002292..23012976hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3810685
hg1910685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354753
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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