A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1n97



Internal ID22815398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:690090..983193hg38UCSC Ensembl
chr1:625470..918573hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38293104
hg19293104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155824, nsv1155993
Samples
Known GenesC1orf170, FAM41C, FAM87B, KLHL17, LINC00115, LINC01128, LOC100130417, LOC100133331, LOC100288069, NOC2L, PLEKHN1, SAMD11
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv1n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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