A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165081



Internal ID21462767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119549532..119549532hg38UCSC Ensembl
chrX:118683495..118683495hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607554
Supporting Variants
SamplesHG03009
Known GenesCXorf56
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165081
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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