A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977551



Internal ID22752486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120873463..120875568hg38UCSC Ensembl
chrX:120007317..120009422hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515274
Samples
Known GenesCT47B1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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