A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447795



Internal ID22113973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26194092..26194218hg38UCSC Ensembl
chrX:26212209..26212335hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759999
Samples
Known GenesMAGEB6
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447795
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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