A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210132



Internal ID22358098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40731433..40731742hg38UCSC Ensembl
chr1:41197105..41197414hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362430
SamplesHG00514
Known GenesNFYC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210132
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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