A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166483



Internal ID21430120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148547139..148547215hg38UCSC Ensembl
chrX:147628660..147628736hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672219
Supporting Variants
SamplesHG00731
Known GenesAFF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166483
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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