A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437956



Internal ID22104137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13713817..13713876hg38UCSC Ensembl
chr10:13755817..13755876hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763491
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437956
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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