A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv228e55



Internal ID22761178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65097016..65603737hg38UCSC Ensembl
chr7:64557394..65068650hg19UCSC Ensembl
chr7:64194829..64706085hg18UCSC Ensembl
chr7:64001544..64512800hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38506722
hg19511257
hg18511257
hg17511257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752168, esv2752169
SamplesSPC_163, BEC_508
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv228e55
Frequency
Sample Size771
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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