A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101075



Internal ID22010308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2228361..2228443hg38UCSC Ensembl
chrX:2146402..2146484hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641782
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101075
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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