A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972472



Internal ID22747407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153304274..153318999hg38UCSC Ensembl
chrX:152569732..152584457hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814726
hg1914726
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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