A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443612



Internal ID22109795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132044702..132044702hg38UCSC Ensembl
chrX:131178730..131178730hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766419
Samples
Known GenesMST4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443612
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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