A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525194



Internal ID22394570
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314856
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525194
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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