A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314219



Internal ID22250457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36650943..36651054hg38UCSC Ensembl
chr4:36652565..36652676hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526302
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314219
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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