A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6646n100



Internal ID22792733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142049538..142071110hg38UCSC Ensembl
chr7:141749338..141770910hg19UCSC Ensembl
chr7:141395807..141417379hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3821573
hg1921573
hg1821573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028792, nsv1023785
Samples
Known GenesMGAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6646n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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