A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167009



Internal ID21430302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30663964..30663964hg38UCSC Ensembl
chrX:30682081..30682081hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604590
Supporting Variants
SamplesHG00731
Known GenesGK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167009
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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