A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138189



Internal ID337372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8037000..8171488hg38UCSC Ensembl
chrX:8005041..8139529hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38134489
hg19134489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739140
Samples
Known GenesMIR651, VCX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138189
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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