A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3736n100



Internal ID20155352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19967927..20016748hg38UCSC Ensembl
chr2:20167688..20216509hg19UCSC Ensembl
chr2:20031169..20079990hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3848822
hg1948822
hg1848822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006404, nsv1005431, nsv1011244
Samples
Known GenesMATN3, WDR35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3736n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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