A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108542



Internal ID22017775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68894630..68894698hg38UCSC Ensembl
chrX:68114473..68114541hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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