A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763634



Internal ID20539494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118053797..118053858hg38UCSC Ensembl
chrX:117187760..117187821hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278814
Samples
Known GenesKLHL13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763634
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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