A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415864



Internal ID195111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76427944..76429937hg38UCSC Ensembl
chrX:75648337..75650330hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg381994
hg191994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740840
Samples
Known GenesMAGEE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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