A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2978n100



Internal ID22789065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51725226..51749378hg38UCSC Ensembl
chr16:51759137..51783289hg19UCSC Ensembl
chr16:50316638..50340790hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3824153
hg1924153
hg1824153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058226, nsv1059733
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)dgv2978n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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