A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759325



Internal ID20535185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122897874..122898009hg38UCSC Ensembl
chrX:122031727..122031862hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759325
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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