A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325692



Internal ID22209423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11096568..11096695hg38UCSC Ensembl
chr1:11156625..11156752hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197418
Supporting Variants
SamplesHG00732
Known GenesEXOSC10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325692
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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