A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv167n97



Internal ID22815564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38721006..38750229hg38UCSC Ensembl
chr2:38948148..38977371hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3829224
hg1929224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155435, nsv1155439
Samples
Known GenesGALM, SRSF7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv167n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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