A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165512



Internal ID21500111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128773940..128773940hg38UCSC Ensembl
chrX:127907918..127907918hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619424
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165512
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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