A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620697



Internal ID21569002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49809378..49809378hg38UCSC Ensembl
chrX:49573981..49573981hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167439
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620697
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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