A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978207



Internal ID22753142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13610621..13612829hg38UCSC Ensembl
chrX:13628740..13630948hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382209
hg192209
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515463
Samples
Known GenesEGFL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978207
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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