A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165182



Internal ID21429660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103894760..103900366hg38UCSC Ensembl
chrX:103149681..103155287hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg385607
hg195607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667319
Supporting Variants
SamplesHG00731
Known GenesMIR1256
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165182
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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