A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953128



Internal ID21373198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85911152..85911152hg38UCSC Ensembl
chrX:85166157..85166157hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15206128
SamplesHG002
Known GenesCHM
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953128
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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