A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7670n100



Internal ID20159286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69417465..69454398hg38UCSC Ensembl
chr9:72032381..72069314hg19UCSC Ensembl
chr9:71222201..71259134hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836934
hg1936934
hg1836934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048256, nsv1041436, nsv1045239
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7670n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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