A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7688n100



Internal ID22793775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93599247..93640465hg38UCSC Ensembl
chr9:96361529..96402747hg19UCSC Ensembl
chr9:95401350..95442568hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3841219
hg1941219
hg1841219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040891, nsv1055035, nsv1044461
Samples
Known GenesPHF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7688n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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