A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021614



Internal ID22083245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73999993..74007305hg38UCSC Ensembl
Outerchr6:73997661..74009077hg38UCSC Ensembl
Innerchr6:74709709..74717021hg19UCSC Ensembl
Outerchr6:74707377..74718793hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811417
hg1911417
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156530
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021614
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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