A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757956



Internal ID20533816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68953112..68953217hg38UCSC Ensembl
chrX:68172955..68173060hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757956
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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