A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106851



Internal ID22016084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46608748..46608837hg38UCSC Ensembl
chrX:46468183..46468272hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648838
Samples
Known GenesSLC9A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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