A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207883



Internal ID22356216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40698486..40699102hg38UCSC Ensembl
chr1:41164158..41164774hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362399
SamplesNA19239
Known GenesNFYC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207883
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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