A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197267



Internal ID22347170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10429403..10429544hg38UCSC Ensembl
chr2:10569529..10569670hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287626, nssv14287625
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197267
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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