A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167975



Internal ID21450380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44865761..44865976hg38UCSC Ensembl
chrX:44725007..44725222hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672356
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167975
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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