A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165536



Internal ID21504789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130989174..130989225hg38UCSC Ensembl
chrX:130123148..130123199hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668359
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165536
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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