A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617212



Internal ID21565517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129850668..129850668hg38UCSC Ensembl
chrX:128984644..128984644hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165690
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617212
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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