A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165541



Internal ID21487147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131327434..131327607hg38UCSC Ensembl
chrX:130461408..130461581hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668346
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165541
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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