A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165128



Internal ID21429632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121199097..121199154hg38UCSC Ensembl
chrX:120332951..120333008hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668098
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165128
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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