A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104940



Internal ID22014174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104250391..104250445hg38UCSC Ensembl
chrX:103495072..103495126hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641794
Samples
Known GenesESX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104940
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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