A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14334270



Internal ID22208069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21862701..21866135hg38UCSC Ensembl
chr10:22151630..22155064hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383435
hg193435
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245245
Supporting Variants
SamplesHG00732
Known GenesDNAJC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14334270
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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