A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761416



Internal ID22095908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160890..6160890hg38UCSC Ensembl
chrX:6078931..6078931hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442610
Supporting Variants
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761416
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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