A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971118



Internal ID22746053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15644011..15656296hg38UCSC Ensembl
chrX:15662134..15674419hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3812286
hg1912286
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515860
Samples
Known GenesTMEM27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971118
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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