A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972549



Internal ID22747484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66710259..66722965hg38UCSC Ensembl
chrX:65930101..65942807hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3812707
hg1912707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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