A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751230



Internal ID20527090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24166687..24168272hg38UCSC Ensembl
chrX:24184804..24186389hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292137
Samples
Known GenesZFX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751230
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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