A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955100



Internal ID22730323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39549733..39549733hg38UCSC Ensembl
chrX:39408987..39408987hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955100
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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