A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138669



Internal ID337853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106024542..106089000hg38UCSC Ensembl
chrX:105268533..105332991hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3864459
hg1964459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741811
Samples
Known GenesSERPINA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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