A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167732



Internal ID21430554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71071574..71071574hg38UCSC Ensembl
chrX:70291424..70291424hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615913
Supporting Variants
SamplesHG00731
Known GenesSNX12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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