A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6163n100



Internal ID22792250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151308573..151343862hg38UCSC Ensembl
chr6:151629708..151664997hg19UCSC Ensembl
chr6:151671401..151706690hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3835290
hg1935290
hg1835290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016584, nsv1018120
Samples
Known GenesAKAP12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6163n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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