A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6566n100



Internal ID22792653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111194962..111626076hg38UCSC Ensembl
chr7:110835018..111266132hg19UCSC Ensembl
chr7:110622254..111053368hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38431115
hg19431115
hg18431115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019130, nsv1021533
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6566n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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