A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022629



Internal ID22084260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121641765..121649281hg38UCSC Ensembl
Outerchr6:121639714..121654417hg38UCSC Ensembl
Innerchr6:121962911..121970427hg19UCSC Ensembl
Outerchr6:121960860..121975563hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3814704
hg1914704
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156579
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022629
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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