A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6779n100



Internal ID22792866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159209715..159327018hg38UCSC Ensembl
chr7:159002404..159119708hg19UCSC Ensembl
chr7:158695165..158812469hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38117304
hg19117305
hg18117305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022261, nsv1027602, nsv1033611, nsv1022868, nsv1032492, nsv1017669, nsv1015328, nsv1024713, nsv1023571
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)dgv6779n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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