A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167857



Internal ID21507882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52627226..52627226hg38UCSC Ensembl
chrX:52656276..52656276hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616587
Supporting Variants
SamplesNA20509
Known GenesSSX8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167857
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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