A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166119



Internal ID21455698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153902761..153902761hg38UCSC Ensembl
chrX:153168215..153168215hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624465
Supporting Variants
SamplesHG02492
Known GenesAVPR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166119
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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