A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443507



Internal ID22109690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151743041..151743041hg38UCSC Ensembl
chrX:150911513..150911513hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764712
Samples
Known GenesCNGA2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443507
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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