A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7504n100



Internal ID22793591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30412520..30565062hg38UCSC Ensembl
chr9:30412518..30565060hg19UCSC Ensembl
chr9:30402518..30555060hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38152543
hg19152543
hg18152543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019695, nsv1020708, nsv1024581, nsv1029183, nsv1018823, nsv1025249, nsv1023399, nsv1020616, nsv1026569
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)dgv7504n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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