A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3733n100



Internal ID22789820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17980692..18018882hg38UCSC Ensembl
chr2:18161958..18200148hg19UCSC Ensembl
chr2:18025439..18063629hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3838191
hg1938191
hg1838191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007980, nsv1011309
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3733n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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