A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316937



Internal ID22233545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108753707..108754047hg38UCSC Ensembl
chr4:109674863..109675203hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202072
Supporting Variants
SamplesHG00733
Known GenesETNPPL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316937
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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