A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106195



Internal ID22015428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49100453..49100511hg38UCSC Ensembl
chrX:48957391..48957449hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638937
Samples
Known GenesWDR45
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106195
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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