A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164849



Internal ID21471132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100723890..100724113hg38UCSC Ensembl
chrX:99978871..99979094hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666966
Supporting Variants
SamplesHG03125
Known GenesSYTL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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