A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442985



Internal ID22109168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101515356..101515356hg38UCSC Ensembl
chrX:100770343..100770343hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766613
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442985
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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