A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416657



Internal ID195878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9814044..9826925hg38UCSC Ensembl
chrX:9782084..9794965hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3812882
hg1912882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739206
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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