A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442987



Internal ID22109170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102559239..102559239hg38UCSC Ensembl
chrX:101814167..101814167hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767558
Samples
Known GenesNXF4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442987
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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