A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971047



Internal ID22745982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102678058..102686791hg38UCSC Ensembl
chrX:101932986..101941719hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg388734
hg198734
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515048
Samples
Known GenesARMCX5-GPRASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971047
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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