A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167798



Internal ID21430576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42285662..42285662hg38UCSC Ensembl
chrX:42144914..42144914hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610773
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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