A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329886



Internal ID22170179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4881150..4881226hg38UCSC Ensembl
chr10:4923342..4923418hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529487
Supporting Variants
SamplesHG00514
Known GenesAKR1C6P
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329886
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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