A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006657



Internal ID22068288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482739..69505361hg38UCSC Ensembl
Outerchr9:69476351..69512262hg38UCSC Ensembl
Innerchr9:72097655..72120277hg19UCSC Ensembl
Outerchr9:72091267..72127178hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3835912
hg1935912
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154509
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006657
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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