A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14317271



Internal ID22190930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173044551..173044605hg38UCSC Ensembl
chr4:173965702..173965756hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525568
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14317271
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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