A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977003



Internal ID22751938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30315066..30329983hg38UCSC Ensembl
chrX:30333183..30348100hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3814918
hg1914918
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977003
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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