A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750914



Internal ID20526774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128773939..128774037hg38UCSC Ensembl
chrX:127907917..127908015hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750914
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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