A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv646088



Internal ID15214622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41404037..41405868hg38UCSC Ensembl
chr4:41406054..41407885hg19UCSC Ensembl
chr4:41100811..41102642hg18UCSC Ensembl
chr4:41246982..41248813hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg381832
hg191832
hg181832
hg171832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv471807
Supporting Variants
Samples
Known GenesLIMCH1
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)nssv646088
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