A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871464



Internal ID22646402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110180512..110195329hg38UCSC Ensembl
chrX:109423740..109438557hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3814818
hg1914818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440158
Samples
Known GenesAMMECR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871464
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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