A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314856



Internal ID22139855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37003181..37003494hg38UCSC Ensembl
chr4:37004803..37005116hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525194
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314856
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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