A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6447n100



Internal ID22792534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67257116..67379052hg38UCSC Ensembl
chr7:66722103..66844039hg19UCSC Ensembl
chr7:66359538..66481474hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38121937
hg19121937
hg18121937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031048, nsv1027702
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6447n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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