A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757360



Internal ID20533220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36371617..36371777hg38UCSC Ensembl
chrX:36389732..36389892hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265457
Samples
Known GenesCXorf30
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757360
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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