A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6527n100



Internal ID20158143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89018127..89047196hg38UCSC Ensembl
chr7:88647441..88676510hg19UCSC Ensembl
chr7:88485377..88514446hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3829070
hg1929070
hg1829070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025619, nsv1025214
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6527n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer