A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969127



Internal ID22744062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103917384..103932520hg38UCSC Ensembl
chrX:103171978..103187094hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3815137
hg1915117
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515062, nssv17515061
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969127
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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