A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975762



Internal ID22750697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23723744..23743568hg38UCSC Ensembl
chrX:23741861..23761685hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3819825
hg1919825
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515994
Samples
Known GenesACOT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975762
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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