A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667291



Internal ID21615598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120463731..120463956hg38UCSC Ensembl
chrX:119597586..119597811hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165111
SamplesHG00513
Known GenesLAMP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667291
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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