A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471738



Internal ID15561330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16124687..16125392hg38UCSC Ensembl
chr5:16124796..16125501hg19UCSC Ensembl
chr5:16177796..16178501hg18UCSC Ensembl
chr5:16177796..16178501hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
hg17706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646019
Samples
Known GenesMARCH11
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)nsv471738
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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