A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165600



Internal ID21492934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321662..125321724hg38UCSC Ensembl
chrX:124455511..124455573hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668947
Supporting Variants
SamplesNA19238
Known GenesLOC100129520
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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