A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761292



Internal ID22095779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152182362..152182362hg38UCSC Ensembl
chrX:151350834..151350834hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443508
Supporting Variants
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761292
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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