A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325665



Internal ID22173681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144172..38144223hg38UCSC Ensembl
chr6:38111948..38111999hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527692
Supporting Variants
SamplesHG00514
Known GenesZFAND3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325665
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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