A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756951



Internal ID20532811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121199108..121199166hg38UCSC Ensembl
chrX:120332962..120333020hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756951
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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