A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167599



Internal ID21430499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47324444..47324444hg38UCSC Ensembl
chrX:47183843..47183843hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618363
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167599
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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