A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv645996



Internal ID15561216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11739326..11739865hg38UCSC Ensembl
chr8:11596835..11597374hg19UCSC Ensembl
chr8:11634244..11634783hg18UCSC Ensembl
chr8:11634244..11634783hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38540
hg19540
hg18540
hg17540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv471715
Supporting Variants
Samples
Known GenesGATA4
MethodOligo aCGH
AnalysisHaploid hybridization data was used to identify genomic intervals showing reduced hybridization signal in comparison to the reference human genome sequence.
PlatformCustom Perlegen arrays
Comments
ReferenceHinds_et_al_2006
Pubmed ID16327809
Accession Number(s)nssv645996
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer