A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437861



Internal ID22104042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7207479..7207530hg38UCSC Ensembl
chr10:7249441..7249492hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758891
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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