A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614973



Internal ID21563278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140771266..140771266hg38UCSC Ensembl
chrX:139853431..139853431hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165825
SamplesHG00512
Known GenesLINC00632
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614973
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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