A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665124



Internal ID21613429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127625450..127752681hg38UCSC Ensembl
chrX:126759431..126886662hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38127232
hg19127232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165480
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665124
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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