A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168199



Internal ID21461568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63546338..63546413hg38UCSC Ensembl
chrX:62766218..62766293hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665658
Supporting Variants
SamplesHG02818
Known GenesLOC92249
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168199
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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