A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8172



Internal ID15535692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:155401786..155417170hg38UCSC Ensembl
Outerchr5:154781346..154796730hg19UCSC Ensembl
Outerchr5:154761539..154776923hg18UCSC Ensembl
Outerchr5:154761539..154776923hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3815385
hg1915385
hg1815385
hg1715385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5083
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv8172
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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