A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362399



Internal ID22277684
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207883
Supporting Variants
SamplesNA19239
Known GenesNFYC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362399
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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