A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165181



Internal ID21467309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103802254..103802254hg38UCSC Ensembl
chrX:103057183..103057183hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621943
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165181
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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