A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7393n100



Internal ID22793480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7730407..7773114hg38UCSC Ensembl
chr9:7730407..7773114hg19UCSC Ensembl
chr9:7720407..7763114hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3842708
hg1942708
hg1842708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015192, nsv1022474, nsv1017021, nsv1034997, nsv1025200, nsv1016692, nsv1035009
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)dgv7393n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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