A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165953



Internal ID21411413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150382868..150383203hg38UCSC Ensembl
chrX:149551136..149551471hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668966
Supporting Variants
SamplesHG00513
Known GenesMAMLD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165953
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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