A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007610



Internal ID22069241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32766328..33169970hg38UCSC Ensembl
Outerchr2:32760381..33175904hg38UCSC Ensembl
Innerchr2:32991395..33395037hg19UCSC Ensembl
Outerchr2:32985448..33400971hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38415524
hg19415524
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155215
Supporting Variants
Samples
Known GenesLINC00486, LOC100271832, LTBP1, TTC27
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007610
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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