A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664587



Internal ID21612892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120296570..120297167hg38UCSC Ensembl
chrX:119430425..119431022hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165101
SamplesNA19239
Known GenesTMEM255A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664587
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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